Name: rs6850422
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs6850422

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:15680814 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.362175 (95864/264690, TOPMED)
C=0.358324 (49893/139240, GnomAD)
C=0.34582 (13274/38384, ALFA) (+ 15 more)
C=0.49547 (14001/28258, 14KJPN)
C=0.48974 (8208/16760, 8.3KJPN)
C=0.3943 (2525/6404, 1000G_30x)
C=0.3966 (1986/5008, 1000G)
C=0.3542 (1586/4478, Estonian)
C=0.3298 (1271/3854, ALSPAC)
C=0.3409 (1264/3708, TWINSUK)
C=0.4137 (1212/2930, KOREAN)
C=0.3827 (718/1876, HapMap)
C=0.370 (222/600, NorthernSweden)
C=0.276 (120/434, SGDP_PRJ)
C=0.426 (92/216, Qatari)
C=0.358 (76/212, Vietnamese)
C=0.25 (14/56, Siberian)
C=0.28 (11/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: FAM200B : Intron Variant
FBXL5 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	38384	C=0.34582	T=0.65418
European	Sub	31934	C=0.33989	T=0.66011
African	Sub	4110	C=0.3749	T=0.6251
African Others	Sub	148	C=0.365	T=0.635
African American	Sub	3962	C=0.3753	T=0.6247
Asian	Sub	168	C=0.470	T=0.530
East Asian	Sub	140	C=0.450	T=0.550
Other Asian	Sub	28	C=0.57	T=0.43
Latin American 1	Sub	166	C=0.367	T=0.633
Latin American 2	Sub	668	C=0.361	T=0.639
South Asian	Sub	98	C=0.49	T=0.51
Other	Sub	1240	C=0.3629	T=0.6371

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	C=0.362175	T=0.637825
gnomAD - Genomes	Global	Study-wide	139240	C=0.358324	T=0.641676
gnomAD - Genomes	European	Sub	75284	C=0.34030	T=0.65970
gnomAD - Genomes	African	Sub	41810	C=0.38723	T=0.61277
gnomAD - Genomes	American	Sub	13562	C=0.36720	T=0.63280
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	C=0.3171	T=0.6829
gnomAD - Genomes	East Asian	Sub	3124	C=0.4036	T=0.5964
gnomAD - Genomes	Other	Sub	2136	C=0.3694	T=0.6306
Allele Frequency Aggregator	Total	Global	38384	C=0.34582	T=0.65418
Allele Frequency Aggregator	European	Sub	31934	C=0.33989	T=0.66011
Allele Frequency Aggregator	African	Sub	4110	C=0.3749	T=0.6251
Allele Frequency Aggregator	Other	Sub	1240	C=0.3629	T=0.6371
Allele Frequency Aggregator	Latin American 2	Sub	668	C=0.361	T=0.639
Allele Frequency Aggregator	Asian	Sub	168	C=0.470	T=0.530
Allele Frequency Aggregator	Latin American 1	Sub	166	C=0.367	T=0.633
Allele Frequency Aggregator	South Asian	Sub	98	C=0.49	T=0.51
14KJPN	JAPANESE	Study-wide	28258	C=0.49547	T=0.50453
8.3KJPN	JAPANESE	Study-wide	16760	C=0.48974	T=0.51026
1000Genomes_30x	Global	Study-wide	6404	C=0.3943	T=0.6057
1000Genomes_30x	African	Sub	1786	C=0.4043	T=0.5957
1000Genomes_30x	Europe	Sub	1266	C=0.3578	T=0.6422
1000Genomes_30x	South Asian	Sub	1202	C=0.4842	T=0.5158
1000Genomes_30x	East Asian	Sub	1170	C=0.3803	T=0.6197
1000Genomes_30x	American	Sub	980	C=0.330	T=0.670
1000Genomes	Global	Study-wide	5008	C=0.3966	T=0.6034
1000Genomes	African	Sub	1322	C=0.3964	T=0.6036
1000Genomes	East Asian	Sub	1008	C=0.3938	T=0.6062
1000Genomes	Europe	Sub	1006	C=0.3598	T=0.6402
1000Genomes	South Asian	Sub	978	C=0.480	T=0.520
1000Genomes	American	Sub	694	C=0.337	T=0.663
Genetic variation in the Estonian population	Estonian	Study-wide	4478	C=0.3542	T=0.6458
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.3298	T=0.6702
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.3409	T=0.6591
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.4137	T=0.5863
HapMap	Global	Study-wide	1876	C=0.3827	T=0.6173
HapMap	American	Sub	766	C=0.376	T=0.624
HapMap	African	Sub	684	C=0.373	T=0.627
HapMap	Asian	Sub	252	C=0.401	T=0.599
HapMap	Europe	Sub	174	C=0.425	T=0.575
Northern Sweden	ACPOP	Study-wide	600	C=0.370	T=0.630
SGDP_PRJ	Global	Study-wide	434	C=0.276	T=0.724
Qatari	Global	Study-wide	216	C=0.426	T=0.574
A Vietnamese Genetic Variation Database	Global	Study-wide	212	C=0.358	T=0.642
Siberian	Global	Study-wide	56	C=0.25	T=0.75
The Danish reference pan genome	Danish	Study-wide	40	C=0.28	T=0.72

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 4	NC_000004.12:g.15680814C>T
GRCh37.p13 chr 4	NC_000004.11:g.15682437C>T

Gene: FAM200B, family with sequence similarity 200 member B (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
FAM200B transcript	NM_001145191.2:c.	N/A	Genic Upstream Transcript Variant
FAM200B transcript variant X12	XM_047450110.1:c.-852-403… XM_047450110.1:c.-852-4036C>T	N/A	Intron Variant
FAM200B transcript variant X13	XM_047450112.1:c.-852-403… XM_047450112.1:c.-852-4036C>T	N/A	Intron Variant
FAM200B transcript variant X3	XM_017008048.2:c.	N/A	Genic Upstream Transcript Variant
FAM200B transcript variant X6	XM_024453999.2:c.	N/A	Genic Upstream Transcript Variant
FAM200B transcript variant X7	XM_024454000.2:c.	N/A	Genic Upstream Transcript Variant
FAM200B transcript variant X10	XM_024454001.2:c.	N/A	Genic Upstream Transcript Variant
FAM200B transcript variant X11	XM_024454003.2:c.	N/A	Genic Upstream Transcript Variant
FAM200B transcript variant X14	XM_024454005.2:c.	N/A	Genic Upstream Transcript Variant
FAM200B transcript variant X15	XM_024454006.2:c.	N/A	Genic Upstream Transcript Variant
FAM200B transcript variant X16	XM_024454008.2:c.	N/A	Genic Upstream Transcript Variant
FAM200B transcript variant X18	XM_024454009.2:c.	N/A	Genic Upstream Transcript Variant
FAM200B transcript variant X19	XM_024454010.2:c.	N/A	Genic Upstream Transcript Variant
FAM200B transcript variant X22	XM_024454011.2:c.	N/A	Genic Upstream Transcript Variant
FAM200B transcript variant X1	XM_047450103.1:c.	N/A	Genic Upstream Transcript Variant
FAM200B transcript variant X2	XM_047450104.1:c.	N/A	Genic Upstream Transcript Variant
FAM200B transcript variant X4	XM_047450106.1:c.	N/A	Genic Upstream Transcript Variant
FAM200B transcript variant X5	XM_047450107.1:c.	N/A	Genic Upstream Transcript Variant
FAM200B transcript variant X8	XM_047450108.1:c.	N/A	Genic Upstream Transcript Variant
FAM200B transcript variant X9	XM_047450109.1:c.	N/A	Genic Upstream Transcript Variant
FAM200B transcript variant X17	XM_047450113.1:c.	N/A	Genic Upstream Transcript Variant
FAM200B transcript variant X20	XM_047450114.1:c.	N/A	Genic Upstream Transcript Variant
FAM200B transcript variant X21	XM_047450115.1:c.	N/A	Genic Upstream Transcript Variant
FAM200B transcript variant X23	XM_047450117.1:c.	N/A	Genic Upstream Transcript Variant

Gene: FBXL5, F-box and leucine rich repeat protein 5 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
FBXL5 transcript variant 3	NM_001193534.2:c.	N/A	Genic Upstream Transcript Variant
FBXL5 transcript variant 4	NM_001193535.2:c.	N/A	Genic Upstream Transcript Variant
FBXL5 transcript variant 1	NM_012161.4:c.	N/A	Genic Upstream Transcript Variant
FBXL5 transcript variant 2	NR_036464.2:n.	N/A	Genic Upstream Transcript Variant
FBXL5 transcript variant X5	XM_006713959.4:c.-284+466… XM_006713959.4:c.-284+466G>A	N/A	Intron Variant
FBXL5 transcript variant X10	XM_011513831.3:c.-267+466… XM_011513831.3:c.-267+466G>A	N/A	Intron Variant
FBXL5 transcript variant X16	XM_017008019.3:c.-892+466… XM_017008019.3:c.-892+466G>A	N/A	Intron Variant
FBXL5 transcript variant X1	XM_047450049.1:c.-281+466… XM_047450049.1:c.-281+466G>A	N/A	Intron Variant
FBXL5 transcript variant X2	XM_047450050.1:c.-932+539… XM_047450050.1:c.-932+539G>A	N/A	Intron Variant
FBXL5 transcript variant X3	XM_047450051.1:c.-946+466… XM_047450051.1:c.-946+466G>A	N/A	Intron Variant
FBXL5 transcript variant X4	XM_047450052.1:c.-949+466… XM_047450052.1:c.-949+466G>A	N/A	Intron Variant
FBXL5 transcript variant X6	XM_047450053.1:c.-270+466… XM_047450053.1:c.-270+466G>A	N/A	Intron Variant
FBXL5 transcript variant X7	XM_047450054.1:c.-267+466… XM_047450054.1:c.-267+466G>A	N/A	Intron Variant
FBXL5 transcript variant X8	XM_047450055.1:c.-270+539… XM_047450055.1:c.-270+539G>A	N/A	Intron Variant
FBXL5 transcript variant X9	XM_047450056.1:c.-267+539… XM_047450056.1:c.-267+539G>A	N/A	Intron Variant
FBXL5 transcript variant X11	XM_047450057.1:c.-284+466… XM_047450057.1:c.-284+466G>A	N/A	Intron Variant
FBXL5 transcript variant X12	XM_047450058.1:c.-281+466… XM_047450058.1:c.-281+466G>A	N/A	Intron Variant
FBXL5 transcript variant X13	XM_047450059.1:c.-281+539… XM_047450059.1:c.-281+539G>A	N/A	Intron Variant
FBXL5 transcript variant X14	XM_047450060.1:c.-935+466… XM_047450060.1:c.-935+466G>A	N/A	Intron Variant
FBXL5 transcript variant X15	XM_047450061.1:c.-943+466… XM_047450061.1:c.-943+466G>A	N/A	Intron Variant
FBXL5 transcript variant X17	XM_011513833.3:c.	N/A	Genic Upstream Transcript Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	C=	T
GRCh38.p14 chr 4	NC_000004.12:g.15680814=	NC_000004.12:g.15680814C>T
GRCh37.p13 chr 4	NC_000004.11:g.15682437=	NC_000004.11:g.15682437C>T
FBXL5 transcript variant X5	XM_006713959.4:c.-284+466=	XM_006713959.4:c.-284+466G>A
FBXL5 transcript variant X10	XM_011513831.3:c.-267+466=	XM_011513831.3:c.-267+466G>A
FBXL5 transcript variant X16	XM_017008019.3:c.-892+466=	XM_017008019.3:c.-892+466G>A
FBXL5 transcript variant X1	XM_047450049.1:c.-281+466=	XM_047450049.1:c.-281+466G>A
FBXL5 transcript variant X2	XM_047450050.1:c.-932+539=	XM_047450050.1:c.-932+539G>A
FBXL5 transcript variant X3	XM_047450051.1:c.-946+466=	XM_047450051.1:c.-946+466G>A
FBXL5 transcript variant X4	XM_047450052.1:c.-949+466=	XM_047450052.1:c.-949+466G>A
FBXL5 transcript variant X6	XM_047450053.1:c.-270+466=	XM_047450053.1:c.-270+466G>A
FBXL5 transcript variant X7	XM_047450054.1:c.-267+466=	XM_047450054.1:c.-267+466G>A
FBXL5 transcript variant X8	XM_047450055.1:c.-270+539=	XM_047450055.1:c.-270+539G>A
FBXL5 transcript variant X9	XM_047450056.1:c.-267+539=	XM_047450056.1:c.-267+539G>A
FBXL5 transcript variant X11	XM_047450057.1:c.-284+466=	XM_047450057.1:c.-284+466G>A
FBXL5 transcript variant X12	XM_047450058.1:c.-281+466=	XM_047450058.1:c.-281+466G>A
FBXL5 transcript variant X13	XM_047450059.1:c.-281+539=	XM_047450059.1:c.-281+539G>A
FBXL5 transcript variant X14	XM_047450060.1:c.-935+466=	XM_047450060.1:c.-935+466G>A
FBXL5 transcript variant X15	XM_047450061.1:c.-943+466=	XM_047450061.1:c.-943+466G>A
FAM200B transcript variant X12	XM_047450110.1:c.-852-4036=	XM_047450110.1:c.-852-4036C>T
FAM200B transcript variant X13	XM_047450112.1:c.-852-4036=	XM_047450112.1:c.-852-4036C>T

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

83 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BCM_SSAHASNP	ss10173721	Jul 11, 2003 (116)
2	CSHL-HAPMAP	ss20224469	Feb 28, 2004 (123)
3	SSAHASNP	ss22186448	Apr 05, 2004 (123)
4	PERLEGEN	ss23307987	Sep 20, 2004 (123)
5	ILLUMINA	ss75191309	Dec 07, 2007 (129)
6	HGSV	ss77790107	Dec 07, 2007 (129)
7	HGSV	ss86137229	Dec 15, 2007 (130)
8	BCMHGSC_JDW	ss92484288	Mar 24, 2008 (129)
9	BGI	ss104044586	Dec 01, 2009 (131)
10	1000GENOMES	ss111845783	Jan 25, 2009 (130)
11	1000GENOMES	ss112948514	Jan 25, 2009 (130)
12	ILLUMINA-UK	ss116887476	Dec 01, 2009 (131)
13	KRIBB_YJKIM	ss119529023	Dec 01, 2009 (131)
14	ENSEMBL	ss139463480	Dec 01, 2009 (131)
15	ENSEMBL	ss143372292	Dec 01, 2009 (131)
16	COMPLETE_GENOMICS	ss161929329	Jul 04, 2010 (132)
17	COMPLETE_GENOMICS	ss163137372	Jul 04, 2010 (132)
18	COMPLETE_GENOMICS	ss166210402	Jul 04, 2010 (132)
19	ILLUMINA	ss174140221	Jul 04, 2010 (132)
20	BUSHMAN	ss198103579	Jul 04, 2010 (132)
21	BCM-HGSC-SUB	ss206280436	Jul 04, 2010 (132)
22	1000GENOMES	ss220763706	Jul 14, 2010 (132)
23	1000GENOMES	ss232275770	Jul 14, 2010 (132)
24	1000GENOMES	ss239592689	Jul 15, 2010 (132)
25	GMI	ss277590109	May 04, 2012 (137)
26	GMI	ss284853817	Apr 25, 2013 (138)
27	PJP	ss293293985	May 09, 2011 (134)
28	ILLUMINA	ss537401554	Sep 08, 2015 (146)
29	TISHKOFF	ss557336613	Apr 25, 2013 (138)
30	SSMP	ss651101274	Apr 25, 2013 (138)
31	EVA-GONL	ss979808105	Aug 21, 2014 (142)
32	JMKIDD_LAB	ss1071306070	Aug 21, 2014 (142)
33	1000GENOMES	ss1308592741	Aug 21, 2014 (142)
34	DDI	ss1429786952	Apr 01, 2015 (144)
35	EVA_GENOME_DK	ss1580432147	Apr 01, 2015 (144)
36	EVA_DECODE	ss1589296731	Apr 01, 2015 (144)
37	EVA_UK10K_ALSPAC	ss1609492390	Apr 01, 2015 (144)
38	EVA_UK10K_TWINSUK	ss1652486423	Apr 01, 2015 (144)
39	EVA_SVP	ss1712654149	Apr 01, 2015 (144)
40	HAMMER_LAB	ss1801058660	Sep 08, 2015 (146)
41	WEILL_CORNELL_DGM	ss1923046682	Feb 12, 2016 (147)
42	GENOMED	ss1969668596	Sep 14, 2016 (149)
43	JJLAB	ss2022096342	Sep 14, 2016 (149)
44	USC_VALOUEV	ss2150206751	Dec 20, 2016 (150)
45	HUMAN_LONGEVITY	ss2260726091	Dec 20, 2016 (150)
46	SYSTEMSBIOZJU	ss2625549252	Nov 08, 2017 (151)
47	GRF	ss2705650895	Nov 08, 2017 (151)
48	ILLUMINA	ss2710999642	Nov 08, 2017 (151)
49	GNOMAD	ss2806083325	Nov 08, 2017 (151)
50	SWEGEN	ss2994206427	Nov 08, 2017 (151)
51	BIOINF_KMB_FNS_UNIBA	ss3024817370	Nov 08, 2017 (151)
52	CSHL	ss3345564646	Nov 08, 2017 (151)
53	ILLUMINA	ss3628909939	Oct 12, 2018 (152)
54	ILLUMINA	ss3638473619	Oct 12, 2018 (152)
55	ILLUMINA	ss3643425916	Oct 12, 2018 (152)
56	URBANLAB	ss3647661572	Oct 12, 2018 (152)
57	EGCUT_WGS	ss3662114329	Jul 13, 2019 (153)
58	EVA_DECODE	ss3711485479	Jul 13, 2019 (153)
59	ACPOP	ss3730891703	Jul 13, 2019 (153)
60	EVA	ss3761448108	Jul 13, 2019 (153)
61	PACBIO	ss3784630466	Jul 13, 2019 (153)
62	PACBIO	ss3790099633	Jul 13, 2019 (153)
63	PACBIO	ss3794974688	Jul 13, 2019 (153)
64	KHV_HUMAN_GENOMES	ss3804581951	Jul 13, 2019 (153)
65	EVA	ss3828390826	Apr 26, 2020 (154)
66	EVA	ss3837628868	Apr 26, 2020 (154)
67	EVA	ss3843063050	Apr 26, 2020 (154)
68	SGDP_PRJ	ss3858308317	Apr 26, 2020 (154)
69	KRGDB	ss3904456914	Apr 26, 2020 (154)
70	TOPMED	ss4604197048	Apr 26, 2021 (155)
71	TOMMO_GENOMICS	ss5164381712	Apr 26, 2021 (155)
72	1000G_HIGH_COVERAGE	ss5258186782	Oct 17, 2022 (156)
73	EVA	ss5347162600	Oct 17, 2022 (156)
74	HUGCELL_USP	ss5457070385	Oct 17, 2022 (156)
75	EVA	ss5507402070	Oct 17, 2022 (156)
76	1000G_HIGH_COVERAGE	ss5538695148	Oct 17, 2022 (156)
77	SANFORD_IMAGENETICS	ss5634432054	Oct 17, 2022 (156)
78	TOMMO_GENOMICS	ss5698081238	Oct 17, 2022 (156)
79	YY_MCH	ss5804793728	Oct 17, 2022 (156)
80	EVA	ss5843607392	Oct 17, 2022 (156)
81	EVA	ss5854096286	Oct 17, 2022 (156)
82	EVA	ss5862306071	Oct 17, 2022 (156)
83	EVA	ss5962809430	Oct 17, 2022 (156)
84	1000Genomes	NC_000004.11 - 15682437	Oct 12, 2018 (152)
85	1000Genomes_30x	NC_000004.12 - 15680814	Oct 17, 2022 (156)
86	The Avon Longitudinal Study of Parents and Children	NC_000004.11 - 15682437	Oct 12, 2018 (152)
87	Genetic variation in the Estonian population	NC_000004.11 - 15682437	Oct 12, 2018 (152)
88	The Danish reference pan genome	NC_000004.11 - 15682437	Apr 26, 2020 (154)
89	gnomAD - Genomes	NC_000004.12 - 15680814	Apr 26, 2021 (155)
90	HapMap	NC_000004.12 - 15680814	Apr 26, 2020 (154)
91	KOREAN population from KRGDB	NC_000004.11 - 15682437	Apr 26, 2020 (154)
92	Northern Sweden	NC_000004.11 - 15682437	Jul 13, 2019 (153)
93	Qatari	NC_000004.11 - 15682437	Apr 26, 2020 (154)
94	SGDP_PRJ	NC_000004.11 - 15682437	Apr 26, 2020 (154)
95	Siberian	NC_000004.11 - 15682437	Apr 26, 2020 (154)
96	8.3KJPN	NC_000004.11 - 15682437	Apr 26, 2021 (155)
97	14KJPN	NC_000004.12 - 15680814	Oct 17, 2022 (156)
98	TopMed	NC_000004.12 - 15680814	Apr 26, 2021 (155)
99	UK 10K study - Twins	NC_000004.11 - 15682437	Oct 12, 2018 (152)
100	A Vietnamese Genetic Variation Database	NC_000004.11 - 15682437	Jul 13, 2019 (153)
101	ALFA	NC_000004.12 - 15680814	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs12650669	Sep 24, 2004 (123)
rs16868235	Oct 07, 2004 (123)
rs60503099	May 26, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss77790107, ss86137229	NC_000004.9:15358705:C:T	NC_000004.12:15680813:C:T	(self)
ss92484288, ss111845783, ss112948514, ss116887476, ss161929329, ss163137372, ss166210402, ss198103579, ss206280436, ss277590109, ss284853817, ss293293985, ss1589296731, ss1712654149, ss3643425916	NC_000004.10:15291534:C:T	NC_000004.12:15680813:C:T	(self)
19945836, 11107145, 7852577, 6597086, 11634308, 4176568, 5088612, 10325297, 2723105, 22351019, 11107145, 2427424, ss220763706, ss232275770, ss239592689, ss537401554, ss557336613, ss651101274, ss979808105, ss1071306070, ss1308592741, ss1429786952, ss1580432147, ss1609492390, ss1652486423, ss1801058660, ss1923046682, ss1969668596, ss2022096342, ss2150206751, ss2625549252, ss2705650895, ss2710999642, ss2806083325, ss2994206427, ss3345564646, ss3628909939, ss3638473619, ss3662114329, ss3730891703, ss3761448108, ss3784630466, ss3790099633, ss3794974688, ss3828390826, ss3837628868, ss3858308317, ss3904456914, ss5164381712, ss5347162600, ss5507402070, ss5634432054, ss5843607392, ss5962809430	NC_000004.11:15682436:C:T	NC_000004.12:15680813:C:T	(self)
26221083, 141380191, 2563828, 31918342, 441574604, 9814783507, ss2260726091, ss3024817370, ss3647661572, ss3711485479, ss3804581951, ss3843063050, ss4604197048, ss5258186782, ss5457070385, ss5538695148, ss5698081238, ss5804793728, ss5854096286, ss5862306071	NC_000004.12:15680813:C:T	NC_000004.12:15680813:C:T	(self)
ss10173721, ss20224469, ss22186448	NT_006316.15:6357794:C:T	NC_000004.12:15680813:C:T	(self)
ss23307987, ss75191309, ss104044586, ss119529023, ss139463480, ss143372292, ss174140221	NT_006316.16:6864233:C:T	NC_000004.12:15680813:C:T	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs6850422

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs6850422