Name: rs78598167
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.

rs78598167

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr18:6110866 (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: T=0.015596 (4128/264690, TOPMED)
T=0.015076 (2112/140092, GnomAD)
T=0.01859 (574/30870, ALFA) (+ 15 more)
T=0.04976 (1406/28258, 14KJPN)
T=0.05054 (847/16760, 8.3KJPN)
T=0.0253 (162/6404, 1000G_30x)
T=0.0284 (142/5008, 1000G)
T=0.0279 (125/4480, Estonian)
T=0.0143 (55/3854, ALSPAC)
T=0.0183 (68/3708, TWINSUK)
T=0.0577 (169/2930, KOREAN)
T=0.020 (20/998, GoNL)
T=0.020 (12/600, NorthernSweden)
T=0.009 (2/216, Qatari)
T=0.084 (18/214, Vietnamese)
C=0.47 (16/34, SGDP_PRJ)
C=0.5 (2/4, Siberian)
T=0.5 (2/4, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: L3MBTL4 : 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	30870	C=0.98141	T=0.01859
European	Sub	24740	C=0.98011	T=0.01989
African	Sub	3168	C=0.9959	T=0.0041
African Others	Sub	124	C=0.992	T=0.008
African American	Sub	3044	C=0.9961	T=0.0039
Asian	Sub	128	C=0.898	T=0.102
East Asian	Sub	100	C=0.91	T=0.09
Other Asian	Sub	28	C=0.86	T=0.14
Latin American 1	Sub	168	C=0.976	T=0.024
Latin American 2	Sub	700	C=0.989	T=0.011
South Asian	Sub	114	C=0.930	T=0.070
Other	Sub	1852	C=0.9806	T=0.0194

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=0.984404	T=0.015596
gnomAD - Genomes	Global	Study-wide	140092	C=0.984924	T=0.015076
gnomAD - Genomes	European	Sub	75906	C=0.98128	T=0.01872
gnomAD - Genomes	African	Sub	41950	C=0.99619	T=0.00381
gnomAD - Genomes	American	Sub	13638	C=0.98834	T=0.01166
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	C=0.9759	T=0.0241
gnomAD - Genomes	East Asian	Sub	3124	C=0.9174	T=0.0826
gnomAD - Genomes	Other	Sub	2152	C=0.9842	T=0.0158
Allele Frequency Aggregator	Total	Global	30870	C=0.98141	T=0.01859
Allele Frequency Aggregator	European	Sub	24740	C=0.98011	T=0.01989
Allele Frequency Aggregator	African	Sub	3168	C=0.9959	T=0.0041
Allele Frequency Aggregator	Other	Sub	1852	C=0.9806	T=0.0194
Allele Frequency Aggregator	Latin American 2	Sub	700	C=0.989	T=0.011
Allele Frequency Aggregator	Latin American 1	Sub	168	C=0.976	T=0.024
Allele Frequency Aggregator	Asian	Sub	128	C=0.898	T=0.102
Allele Frequency Aggregator	South Asian	Sub	114	C=0.930	T=0.070
14KJPN	JAPANESE	Study-wide	28258	C=0.95024	T=0.04976
8.3KJPN	JAPANESE	Study-wide	16760	C=0.94946	T=0.05054
1000Genomes_30x	Global	Study-wide	6404	C=0.9747	T=0.0253
1000Genomes_30x	African	Sub	1786	C=1.0000	T=0.0000
1000Genomes_30x	Europe	Sub	1266	C=0.9810	T=0.0190
1000Genomes_30x	South Asian	Sub	1202	C=0.9567	T=0.0433
1000Genomes_30x	East Asian	Sub	1170	C=0.9359	T=0.0641
1000Genomes_30x	American	Sub	980	C=0.989	T=0.011
1000Genomes	Global	Study-wide	5008	C=0.9716	T=0.0284
1000Genomes	African	Sub	1322	C=1.0000	T=0.0000
1000Genomes	East Asian	Sub	1008	C=0.9306	T=0.0694
1000Genomes	Europe	Sub	1006	C=0.9831	T=0.0169
1000Genomes	South Asian	Sub	978	C=0.953	T=0.047
1000Genomes	American	Sub	694	C=0.987	T=0.013
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.9721	T=0.0279
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.9857	T=0.0143
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.9817	T=0.0183
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.9423	T=0.0577
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.980	T=0.020
Northern Sweden	ACPOP	Study-wide	600	C=0.980	T=0.020
Qatari	Global	Study-wide	216	C=0.991	T=0.009
A Vietnamese Genetic Variation Database	Global	Study-wide	214	C=0.916	T=0.084
SGDP_PRJ	Global	Study-wide	34	C=0.47	T=0.53
Siberian	Global	Study-wide	4	C=0.5	T=0.5

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 18	NC_000018.10:g.6110866C>T
GRCh37.p13 chr 18	NC_000018.9:g.6110865C>T

Gene: L3MBTL4, L3MBTL histone methyl-lysine binding protein 4 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
L3MBTL4 transcript variant 2	NM_001330559.2:c.1200-173… NM_001330559.2:c.1200-17338G>A	N/A	Intron Variant
L3MBTL4 transcript variant 3	NM_001365765.2:c.1200-173… NM_001365765.2:c.1200-17338G>A	N/A	Intron Variant
L3MBTL4 transcript variant 6	NM_001365766.2:c.1200-173… NM_001365766.2:c.1200-17338G>A	N/A	Intron Variant
L3MBTL4 transcript variant 7	NM_001365767.2:c.1200-173… NM_001365767.2:c.1200-17338G>A	N/A	Intron Variant
L3MBTL4 transcript variant 8	NM_001365768.2:c.1200-173… NM_001365768.2:c.1200-17338G>A	N/A	Intron Variant
L3MBTL4 transcript variant 9	NM_001365769.2:c.1200-173… NM_001365769.2:c.1200-17338G>A	N/A	Intron Variant
L3MBTL4 transcript variant 10	NM_001365770.2:c.1200-173… NM_001365770.2:c.1200-17338G>A	N/A	Intron Variant
L3MBTL4 transcript variant 1	NM_173464.4:c.1200-17338G… NM_173464.4:c.1200-17338G>A	N/A	Intron Variant
L3MBTL4 transcript variant 4	NR_158609.2:n.	N/A	Intron Variant
L3MBTL4 transcript variant 5	NR_158610.2:n.	N/A	Intron Variant
L3MBTL4 transcript variant 11	NR_158611.2:n.	N/A	Intron Variant
L3MBTL4 transcript variant X15	XM_006722364.3:c.1200-173… XM_006722364.3:c.1200-17338G>A	N/A	Intron Variant
L3MBTL4 transcript variant X1	XM_011525757.2:c.1200-173… XM_011525757.2:c.1200-17338G>A	N/A	Intron Variant
L3MBTL4 transcript variant X3	XM_011525758.2:c.1200-173… XM_011525758.2:c.1200-17338G>A	N/A	Intron Variant
L3MBTL4 transcript variant X6	XM_011525759.2:c.1200-173… XM_011525759.2:c.1200-17338G>A	N/A	Intron Variant
L3MBTL4 transcript variant X7	XM_011525760.2:c.1200-173… XM_011525760.2:c.1200-17338G>A	N/A	Intron Variant
L3MBTL4 transcript variant X12	XM_011525762.3:c.1200-173… XM_011525762.3:c.1200-17338G>A	N/A	Intron Variant
L3MBTL4 transcript variant X13	XM_011525763.3:c.1200-173… XM_011525763.3:c.1200-17338G>A	N/A	Intron Variant
L3MBTL4 transcript variant X20	XM_011525767.3:c.333-1733… XM_011525767.3:c.333-17338G>A	N/A	Intron Variant
L3MBTL4 transcript variant X11	XM_017026074.2:c.1200-173… XM_017026074.2:c.1200-17338G>A	N/A	Intron Variant
L3MBTL4 transcript variant X2	XM_047437914.1:c.1200-173… XM_047437914.1:c.1200-17338G>A	N/A	Intron Variant
L3MBTL4 transcript variant X4	XM_047437915.1:c.1200-173… XM_047437915.1:c.1200-17338G>A	N/A	Intron Variant
L3MBTL4 transcript variant X5	XM_047437916.1:c.1200-173… XM_047437916.1:c.1200-17338G>A	N/A	Intron Variant
L3MBTL4 transcript variant X8	XM_047437917.1:c.1200-173… XM_047437917.1:c.1200-17338G>A	N/A	Intron Variant
L3MBTL4 transcript variant X9	XM_047437918.1:c.1200-173… XM_047437918.1:c.1200-17338G>A	N/A	Intron Variant
L3MBTL4 transcript variant X10	XM_047437919.1:c.1200-173… XM_047437919.1:c.1200-17338G>A	N/A	Intron Variant
L3MBTL4 transcript variant X14	XM_047437920.1:c.1200-173… XM_047437920.1:c.1200-17338G>A	N/A	Intron Variant
L3MBTL4 transcript variant X18	XM_017026077.2:c.	N/A	Genic Downstream Transcript Variant
L3MBTL4 transcript variant X16	XR_007066252.1:n.	N/A	Genic Downstream Transcript Variant
L3MBTL4 transcript variant X17	XR_007066253.1:n.	N/A	Genic Downstream Transcript Variant
L3MBTL4 transcript variant X19	XR_935072.2:n.	N/A	Genic Downstream 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 18	NC_000018.10:g.6110866=	NC_000018.10:g.6110866C>T
GRCh37.p13 chr 18	NC_000018.9:g.6110865=	NC_000018.9:g.6110865C>T
L3MBTL4 transcript variant 2	NM_001330559.2:c.1200-17338=	NM_001330559.2:c.1200-17338G>A
L3MBTL4 transcript variant 3	NM_001365765.2:c.1200-17338=	NM_001365765.2:c.1200-17338G>A
L3MBTL4 transcript variant 6	NM_001365766.2:c.1200-17338=	NM_001365766.2:c.1200-17338G>A
L3MBTL4 transcript variant 7	NM_001365767.2:c.1200-17338=	NM_001365767.2:c.1200-17338G>A
L3MBTL4 transcript variant 8	NM_001365768.2:c.1200-17338=	NM_001365768.2:c.1200-17338G>A
L3MBTL4 transcript variant 9	NM_001365769.2:c.1200-17338=	NM_001365769.2:c.1200-17338G>A
L3MBTL4 transcript variant 10	NM_001365770.2:c.1200-17338=	NM_001365770.2:c.1200-17338G>A
L3MBTL4 transcript variant 1	NM_173464.3:c.1200-17338=	NM_173464.3:c.1200-17338G>A
L3MBTL4 transcript variant 1	NM_173464.4:c.1200-17338=	NM_173464.4:c.1200-17338G>A
L3MBTL4 transcript variant X1	XM_005258165.1:c.1200-17338=	XM_005258165.1:c.1200-17338G>A
L3MBTL4 transcript variant X6	XM_005258166.1:c.1200-17338=	XM_005258166.1:c.1200-17338G>A
L3MBTL4 transcript variant X3	XM_005258167.1:c.1200-17338=	XM_005258167.1:c.1200-17338G>A
L3MBTL4 transcript variant X4	XM_005258168.1:c.1200-17338=	XM_005258168.1:c.1200-17338G>A
L3MBTL4 transcript variant X5	XM_005258169.1:c.1200-17338=	XM_005258169.1:c.1200-17338G>A
L3MBTL4 transcript variant X15	XM_006722364.3:c.1200-17338=	XM_006722364.3:c.1200-17338G>A
L3MBTL4 transcript variant X1	XM_011525757.2:c.1200-17338=	XM_011525757.2:c.1200-17338G>A
L3MBTL4 transcript variant X3	XM_011525758.2:c.1200-17338=	XM_011525758.2:c.1200-17338G>A
L3MBTL4 transcript variant X6	XM_011525759.2:c.1200-17338=	XM_011525759.2:c.1200-17338G>A
L3MBTL4 transcript variant X7	XM_011525760.2:c.1200-17338=	XM_011525760.2:c.1200-17338G>A
L3MBTL4 transcript variant X12	XM_011525762.3:c.1200-17338=	XM_011525762.3:c.1200-17338G>A
L3MBTL4 transcript variant X13	XM_011525763.3:c.1200-17338=	XM_011525763.3:c.1200-17338G>A
L3MBTL4 transcript variant X20	XM_011525767.3:c.333-17338=	XM_011525767.3:c.333-17338G>A
L3MBTL4 transcript variant X11	XM_017026074.2:c.1200-17338=	XM_017026074.2:c.1200-17338G>A
L3MBTL4 transcript variant X2	XM_047437914.1:c.1200-17338=	XM_047437914.1:c.1200-17338G>A
L3MBTL4 transcript variant X4	XM_047437915.1:c.1200-17338=	XM_047437915.1:c.1200-17338G>A
L3MBTL4 transcript variant X5	XM_047437916.1:c.1200-17338=	XM_047437916.1:c.1200-17338G>A
L3MBTL4 transcript variant X8	XM_047437917.1:c.1200-17338=	XM_047437917.1:c.1200-17338G>A
L3MBTL4 transcript variant X9	XM_047437918.1:c.1200-17338=	XM_047437918.1:c.1200-17338G>A
L3MBTL4 transcript variant X10	XM_047437919.1:c.1200-17338=	XM_047437919.1:c.1200-17338G>A
L3MBTL4 transcript variant X14	XM_047437920.1:c.1200-17338=	XM_047437920.1:c.1200-17338G>A

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#.

56 SubSNP, 17 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BGI	ss103372966	Dec 01, 2009 (131)
2	1000GENOMES	ss237368181	Jul 15, 2010 (132)
3	1000GENOMES	ss243638630	Jul 15, 2010 (132)
4	GMI	ss282888661	May 04, 2012 (137)
5	ILLUMINA	ss483759096	May 04, 2012 (137)
6	ILLUMINA	ss484097887	May 04, 2012 (137)
7	ILLUMINA	ss536288127	Sep 08, 2015 (146)
8	SSMP	ss661302231	Apr 25, 2013 (138)
9	ILLUMINA	ss780525603	Sep 08, 2015 (146)
10	ILLUMINA	ss782494063	Sep 08, 2015 (146)
11	ILLUMINA	ss836017100	Sep 08, 2015 (146)
12	EVA-GONL	ss993455534	Aug 21, 2014 (142)
13	JMKIDD_LAB	ss1081302075	Aug 21, 2014 (142)
14	1000GENOMES	ss1359993613	Aug 21, 2014 (142)
15	EVA_UK10K_ALSPAC	ss1636337819	Apr 01, 2015 (144)
16	EVA_UK10K_TWINSUK	ss1679331852	Apr 01, 2015 (144)
17	EVA_DECODE	ss1697508056	Apr 01, 2015 (144)
18	WEILL_CORNELL_DGM	ss1936926254	Feb 12, 2016 (147)
19	JJLAB	ss2029235422	Sep 14, 2016 (149)
20	USC_VALOUEV	ss2157730719	Dec 20, 2016 (150)
21	HUMAN_LONGEVITY	ss2219548495	Dec 20, 2016 (150)
22	SYSTEMSBIOZJU	ss2629115104	Nov 08, 2017 (151)
23	ILLUMINA	ss2633442232	Nov 08, 2017 (151)
24	GRF	ss2702300634	Nov 08, 2017 (151)
25	GNOMAD	ss2953732977	Nov 08, 2017 (151)
26	SWEGEN	ss3016101727	Nov 08, 2017 (151)
27	CSHL	ss3351901051	Nov 08, 2017 (151)
28	ILLUMINA	ss3627752443	Oct 12, 2018 (152)
29	ILLUMINA	ss3631420280	Oct 12, 2018 (152)
30	ILLUMINA	ss3642014392	Oct 12, 2018 (152)
31	EGCUT_WGS	ss3682957475	Jul 13, 2019 (153)
32	EVA_DECODE	ss3701151728	Jul 13, 2019 (153)
33	ACPOP	ss3742322387	Jul 13, 2019 (153)
34	EVA	ss3755077266	Jul 13, 2019 (153)
35	KHV_HUMAN_GENOMES	ss3820341589	Jul 13, 2019 (153)
36	SGDP_PRJ	ss3886474583	Apr 27, 2020 (154)
37	KRGDB	ss3936280060	Apr 27, 2020 (154)
38	TOPMED	ss5047567553	Apr 27, 2021 (155)
39	TOMMO_GENOMICS	ss5224015275	Apr 27, 2021 (155)
40	EVA	ss5237582190	Apr 27, 2021 (155)
41	1000G_HIGH_COVERAGE	ss5304349927	Oct 16, 2022 (156)
42	EVA	ss5315914122	Oct 16, 2022 (156)
43	EVA	ss5429764742	Oct 16, 2022 (156)
44	HUGCELL_USP	ss5497267673	Oct 16, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5608628175	Oct 16, 2022 (156)
46	SANFORD_IMAGENETICS	ss5624407114	Oct 16, 2022 (156)
47	SANFORD_IMAGENETICS	ss5660777365	Oct 16, 2022 (156)
48	TOMMO_GENOMICS	ss5780740964	Oct 16, 2022 (156)
49	YY_MCH	ss5816837116	Oct 16, 2022 (156)
50	EVA	ss5827192896	Oct 16, 2022 (156)
51	EVA	ss5847481797	Oct 16, 2022 (156)
52	EVA	ss5847813369	Oct 16, 2022 (156)
53	EVA	ss5851949974	Oct 16, 2022 (156)
54	EVA	ss5873061086	Oct 16, 2022 (156)
55	EVA	ss5952177394	Oct 16, 2022 (156)
56	EVA	ss5979519616	Oct 16, 2022 (156)
57	1000Genomes	NC_000018.9 - 6110865	Oct 12, 2018 (152)
58	1000Genomes_30x	NC_000018.10 - 6110866	Oct 16, 2022 (156)
59	The Avon Longitudinal Study of Parents and Children	NC_000018.9 - 6110865	Oct 12, 2018 (152)
60	Genetic variation in the Estonian population	NC_000018.9 - 6110865	Oct 12, 2018 (152)
61	gnomAD - Genomes	NC_000018.10 - 6110866	Apr 27, 2021 (155)
62	Genome of the Netherlands Release 5	NC_000018.9 - 6110865	Apr 27, 2020 (154)
63	KOREAN population from KRGDB	NC_000018.9 - 6110865	Apr 27, 2020 (154)
64	Northern Sweden	NC_000018.9 - 6110865	Jul 13, 2019 (153)
65	Qatari	NC_000018.9 - 6110865	Apr 27, 2020 (154)
66	SGDP_PRJ	NC_000018.9 - 6110865	Apr 27, 2020 (154)
67	Siberian	NC_000018.9 - 6110865	Apr 27, 2020 (154)
68	8.3KJPN	NC_000018.9 - 6110865	Apr 27, 2021 (155)
69	14KJPN	NC_000018.10 - 6110866	Oct 16, 2022 (156)
70	TopMed	NC_000018.10 - 6110866	Apr 27, 2021 (155)
71	UK 10K study - Twins	NC_000018.9 - 6110865	Oct 12, 2018 (152)
72	A Vietnamese Genetic Variation Database	NC_000018.9 - 6110865	Jul 13, 2019 (153)
73	ALFA	NC_000018.10 - 6110866	Apr 27, 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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss282888661, ss483759096, ss1697508056	NC_000018.8:6100864:C:T	NC_000018.10:6110865:C:T	(self)
73286544, 40608395, 28695723, 18090482, 43457454, 15607252, 18968176, 38491563, 10247073, 81984582, 40608395, 8976043, ss237368181, ss243638630, ss484097887, ss536288127, ss661302231, ss780525603, ss782494063, ss836017100, ss993455534, ss1081302075, ss1359993613, ss1636337819, ss1679331852, ss1936926254, ss2029235422, ss2157730719, ss2629115104, ss2633442232, ss2702300634, ss2953732977, ss3016101727, ss3351901051, ss3627752443, ss3631420280, ss3642014392, ss3682957475, ss3742322387, ss3755077266, ss3886474583, ss3936280060, ss5224015275, ss5237582190, ss5315914122, ss5429764742, ss5624407114, ss5660777365, ss5827192896, ss5847481797, ss5847813369, ss5952177394, ss5979519616	NC_000018.9:6110864:C:T	NC_000018.10:6110865:C:T	(self)
96154110, 517063615, 114578068, 263113216, 13950016821, ss2219548495, ss3701151728, ss3820341589, ss5047567553, ss5304349927, ss5497267673, ss5608628175, ss5780740964, ss5816837116, ss5851949974, ss5873061086	NC_000018.10:6110865:C:T	NC_000018.10:6110865:C:T	(self)
ss103372966	NT_010859.14:6100864:C:T	NC_000018.10:6110865: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 rs78598167

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
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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

rs78598167