Name: rs73390944
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.

rs73390944

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr22:29696706 (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: A>C / A>G
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.06907 (1362/19718, ALFA)
G=0.1488 (953/6404, 1000G_30x)
G=0.1452 (727/5008, 1000G) (+ 11 more)
G=0.1574 (705/4480, Estonian)
G=0.1297 (500/3854, ALSPAC)
G=0.1286 (477/3708, TWINSUK)
G=0.0363 (106/2922, KOREAN)
G=0.130 (130/998, GoNL)
G=0.128 (77/600, NorthernSweden)
G=0.088 (19/216, Qatari)
G=0.104 (22/212, Vietnamese)
A=0.457 (53/116, SGDP_PRJ)
G=0.10 (4/40, GENOME_DK)
A=0.44 (8/18, Siberian)

Clinical Significance: Reported in ClinVar
Gene : Consequence: NF2 : Non Coding Transcript 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	19718	A=0.93093	C=0.00000, G=0.06907
European	Sub	16404	A=0.91911	C=0.00000, G=0.08089
African	Sub	1966	A=0.9980	C=0.0000, G=0.0020
African Others	Sub	58	A=1.00	C=0.00, G=0.00
African American	Sub	1908	A=0.9979	C=0.0000, G=0.0021
Asian	Sub	90	A=1.00	C=0.00, G=0.00
East Asian	Sub	68	A=1.00	C=0.00, G=0.00
Other Asian	Sub	22	A=1.00	C=0.00, G=0.00
Latin American 1	Sub	130	A=1.000	C=0.000, G=0.000
Latin American 2	Sub	438	A=1.000	C=0.000, G=0.000
South Asian	Sub	76	A=1.00	C=0.00, G=0.00
Other	Sub	614	A=0.950	C=0.000, G=0.050

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
Allele Frequency Aggregator	Total	Global	19718	A=0.93093	C=0.00000, G=0.06907
Allele Frequency Aggregator	European	Sub	16404	A=0.91911	C=0.00000, G=0.08089
Allele Frequency Aggregator	African	Sub	1966	A=0.9980	C=0.0000, G=0.0020
Allele Frequency Aggregator	Other	Sub	614	A=0.950	C=0.000, G=0.050
Allele Frequency Aggregator	Latin American 2	Sub	438	A=1.000	C=0.000, G=0.000
Allele Frequency Aggregator	Latin American 1	Sub	130	A=1.000	C=0.000, G=0.000
Allele Frequency Aggregator	Asian	Sub	90	A=1.00	C=0.00, G=0.00
Allele Frequency Aggregator	South Asian	Sub	76	A=1.00	C=0.00, G=0.00
1000Genomes_30x	Global	Study-wide	6404	A=0.8512	G=0.1488
1000Genomes_30x	African	Sub	1786	A=0.7755	G=0.2245
1000Genomes_30x	Europe	Sub	1266	A=0.9013	G=0.0987
1000Genomes_30x	South Asian	Sub	1202	A=0.8195	G=0.1805
1000Genomes_30x	East Asian	Sub	1170	A=0.9342	G=0.0658
1000Genomes_30x	American	Sub	980	A=0.864	G=0.136
1000Genomes	Global	Study-wide	5008	A=0.8548	G=0.1452
1000Genomes	African	Sub	1322	A=0.7799	G=0.2201
1000Genomes	East Asian	Sub	1008	A=0.9375	G=0.0625
1000Genomes	Europe	Sub	1006	A=0.8976	G=0.1024
1000Genomes	South Asian	Sub	978	A=0.817	G=0.183
1000Genomes	American	Sub	694	A=0.869	G=0.131
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.8426	G=0.1574
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.8703	G=0.1297
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.8714	G=0.1286
KOREAN population from KRGDB	KOREAN	Study-wide	2922	A=0.9637	G=0.0363
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.870	G=0.130
Northern Sweden	ACPOP	Study-wide	600	A=0.872	G=0.128
Qatari	Global	Study-wide	216	A=0.912	G=0.088
A Vietnamese Genetic Variation Database	Global	Study-wide	212	A=0.896	G=0.104
SGDP_PRJ	Global	Study-wide	116	A=0.457	G=0.543
The Danish reference pan genome	Danish	Study-wide	40	A=0.90	G=0.10
Siberian	Global	Study-wide	18	A=0.44	G=0.56

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 22	NC_000022.11:g.29696706A>C
GRCh38.p14 chr 22	NC_000022.11:g.29696706A>G
GRCh37.p13 chr 22	NC_000022.10:g.30092695A>C
GRCh37.p13 chr 22	NC_000022.10:g.30092695A>G
MERLIN RefSeqGene (LRG_511)	NG_009057.1:g.98151A>C
MERLIN RefSeqGene (LRG_511)	NG_009057.1:g.98151A>G

Gene: NF2, NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NF2 transcript variant 2	NM_016418.5:c.*1964=	N/A	3 Prime UTR Variant
NF2 transcript variant 6	NM_181829.3:c.*1964=	N/A	3 Prime UTR Variant
NF2 transcript variant 8	NM_181832.3:c.*1979=	N/A	3 Prime UTR Variant
NF2 transcript variant 5	NM_181828.3:c.*1964=	N/A	3 Prime UTR Variant
NF2 transcript variant 7	NM_181830.3:c.*1964=	N/A	3 Prime UTR Variant
NF2 transcript variant 1	NM_000268.4:c.*1904=	N/A	3 Prime UTR Variant
NF2 transcript variant 9	NM_181833.3:c.*1904=	N/A	3 Prime UTR Variant
NF2 transcript variant 12	NM_181825.3:c.	N/A	Genic Downstream Transcript Variant
NF2 transcript variant 13	NM_181831.3:c.	N/A	Genic Downstream Transcript Variant
NF2 transcript variant 14	NR_156186.2:n.4174A>C	N/A	Non Coding Transcript Variant
NF2 transcript variant 14	NR_156186.2:n.4174A>G	N/A	Non Coding Transcript Variant
NF2 transcript variant X1	XM_017028809.3:c.*1904=	N/A	3 Prime UTR Variant
NF2 transcript variant X2	XM_047441386.1:c.*1979=	N/A	3 Prime UTR 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.

Allele: G (allele ID: 352361 )

ClinVar Accession	Disease Names	Clinical Significance
RCV000334760.3	Neurofibromatosis, type 2	Benign

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	A=	C	G
GRCh38.p14 chr 22	NC_000022.11:g.29696706=	NC_000022.11:g.29696706A>C	NC_000022.11:g.29696706A>G
GRCh37.p13 chr 22	NC_000022.10:g.30092695=	NC_000022.10:g.30092695A>C	NC_000022.10:g.30092695A>G
MERLIN RefSeqGene (LRG_511)	NG_009057.1:g.98151=	NG_009057.1:g.98151A>C	NG_009057.1:g.98151A>G
NF2 transcript variant 2	NM_016418.5:c.*1964=	NM_016418.5:c.*1964A>C	NM_016418.5:c.*1964A>G
NF2 transcript variant 1	NM_000268.4:c.*1904=	NM_000268.4:c.*1904A>C	NM_000268.4:c.*1904A>G
NF2 transcript variant 1	NM_000268.3:c.*1904=	NM_000268.3:c.*1904A>C	NM_000268.3:c.*1904A>G
NF2 transcript variant 8	NM_181832.3:c.*1979=	NM_181832.3:c.*1979A>C	NM_181832.3:c.*1979A>G
NF2 transcript variant 8	NM_181832.2:c.*1979=	NM_181832.2:c.*1979A>C	NM_181832.2:c.*1979A>G
NF2 transcript variant 6	NM_181829.3:c.*1964=	NM_181829.3:c.*1964A>C	NM_181829.3:c.*1964A>G
NF2 transcript variant 6	NM_181829.2:c.*1964=	NM_181829.2:c.*1964A>C	NM_181829.2:c.*1964A>G
NF2 transcript variant 5	NM_181828.3:c.*1964=	NM_181828.3:c.*1964A>C	NM_181828.3:c.*1964A>G
NF2 transcript variant 5	NM_181828.2:c.*1964=	NM_181828.2:c.*1964A>C	NM_181828.2:c.*1964A>G
NF2 transcript variant 7	NM_181830.3:c.*1964=	NM_181830.3:c.*1964A>C	NM_181830.3:c.*1964A>G
NF2 transcript variant 7	NM_181830.2:c.*1964=	NM_181830.2:c.*1964A>C	NM_181830.2:c.*1964A>G
NF2 transcript variant 9	NM_181833.3:c.*1904=	NM_181833.3:c.*1904A>C	NM_181833.3:c.*1904A>G
NF2 transcript variant 9	NM_181833.2:c.*1904=	NM_181833.2:c.*1904A>C	NM_181833.2:c.*1904A>G
NF2 transcript variant 18	NM_001407056.1:c.*1964=	NM_001407056.1:c.*1964A>C	NM_001407056.1:c.*1964A>G
NF2 transcript variant 27	NM_001407065.1:c.*1964=	NM_001407065.1:c.*1964A>C	NM_001407065.1:c.*1964A>G
NF2 transcript variant 14	NM_001407053.1:c.*1904=	NM_001407053.1:c.*1904A>C	NM_001407053.1:c.*1904A>G
NF2 transcript variant 23	NM_001407067.1:c.*1964=	NM_001407067.1:c.*1964A>C	NM_001407067.1:c.*1964A>G
NF2 transcript variant 20	NM_001407058.1:c.*1979=	NM_001407058.1:c.*1979A>C	NM_001407058.1:c.*1979A>G
NF2 transcript variant 21	NM_001407059.1:c.*1964=	NM_001407059.1:c.*1964A>C	NM_001407059.1:c.*1964A>G
NF2 transcript variant 16	NM_001407054.1:c.*1904=	NM_001407054.1:c.*1904A>C	NM_001407054.1:c.*1904A>G
NF2 transcript variant 17	NM_001407055.1:c.*1904=	NM_001407055.1:c.*1904A>C	NM_001407055.1:c.*1904A>G
NF2 transcript variant 19	NM_001407057.1:c.*1904=	NM_001407057.1:c.*1904A>C	NM_001407057.1:c.*1904A>G
NF2 transcript variant 22	NM_001407060.1:c.*1897=	NM_001407060.1:c.*1897A>C	NM_001407060.1:c.*1897A>G
NF2 transcript variant 25	NM_001407063.1:c.*1979=	NM_001407063.1:c.*1979A>C	NM_001407063.1:c.*1979A>G
NF2 transcript variant 24	NM_001407062.1:c.*1904=	NM_001407062.1:c.*1904A>C	NM_001407062.1:c.*1904A>G
NF2 transcript variant 26	NM_001407064.1:c.*1897=	NM_001407064.1:c.*1897A>C	NM_001407064.1:c.*1897A>G
NF2 transcript variant 28	NR_176267.1:n.3077=	NR_176267.1:n.3077A>C	NR_176267.1:n.3077A>G
NF2 transcript variant X1	XM_017028809.3:c.*1904=	XM_017028809.3:c.*1904A>C	XM_017028809.3:c.*1904A>G
NF2 transcript variant X1	XM_017028809.1:c.*1904=	XM_017028809.1:c.*1904A>C	XM_017028809.1:c.*1904A>G
NF2 transcript variant 14	NR_156186.2:n.4174=	NR_156186.2:n.4174A>C	NR_156186.2:n.4174A>G
NF2 transcript variant 3	NM_181826.1:c.*3619=	NM_181826.1:c.*3619A>C	NM_181826.1:c.*3619A>G
NF2 transcript variant 14	NR_156186.1:n.4251=	NR_156186.1:n.4251A>C	NR_156186.1:n.4251A>G
NF2 transcript variant 4	NM_181827.1:c.*3483=	NM_181827.1:c.*3483A>C	NM_181827.1:c.*3483A>G
NF2 transcript variant X2	XM_047441386.1:c.*1979=	XM_047441386.1:c.*1979A>C	XM_047441386.1:c.*1979A>G
NF2 transcript variant 11	NM_181835.1:c.*1965=	NM_181835.1:c.*1965A>C	NM_181835.1:c.*1965A>G
NF2 transcript variant 10	NM_181834.1:c.*2048=	NM_181834.1:c.*2048A>C	NM_181834.1:c.*2048A>G

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#.

64 SubSNP, 24 Frequency, 1 ClinVar submissions

No	Submitter	Submission ID	Date (Build)
1	1000GENOMES	ss114130694	Feb 14, 2009 (130)
2	COMPLETE_GENOMICS	ss169089392	Jul 04, 2010 (132)
3	COMPLETE_GENOMICS	ss171913599	Jul 04, 2010 (132)
4	1000GENOMES	ss228654923	Jul 14, 2010 (132)
5	1000GENOMES	ss238049785	Jul 15, 2010 (132)
6	1000GENOMES	ss244173493	Jul 15, 2010 (132)
7	BL	ss255877144	May 09, 2011 (134)
8	ILLUMINA	ss483576649	May 04, 2012 (137)
9	ILLUMINA	ss484301328	May 04, 2012 (137)
10	SSMP	ss662537823	Apr 25, 2013 (138)
11	ILLUMINA	ss782231768	Aug 21, 2014 (142)
12	EVA-GONL	ss995299595	Aug 21, 2014 (142)
13	JMKIDD_LAB	ss1082621861	Aug 21, 2014 (142)
14	1000GENOMES	ss1366974338	Aug 21, 2014 (142)
15	DDI	ss1429242422	Apr 01, 2015 (144)
16	EVA_GENOME_DK	ss1579732534	Apr 01, 2015 (144)
17	EVA_UK10K_ALSPAC	ss1639891824	Apr 01, 2015 (144)
18	EVA_UK10K_TWINSUK	ss1682885857	Apr 01, 2015 (144)
19	EVA_DECODE	ss1699368690	Apr 01, 2015 (144)
20	HAMMER_LAB	ss1809766909	Sep 08, 2015 (146)
21	WEILL_CORNELL_DGM	ss1938865871	Feb 12, 2016 (147)
22	GENOMED	ss1969262390	Jul 19, 2016 (147)
23	JJLAB	ss2030204610	Sep 14, 2016 (149)
24	ILLUMINA	ss2094922391	Dec 20, 2016 (150)
25	ILLUMINA	ss2095121849	Dec 20, 2016 (150)
26	USC_VALOUEV	ss2158820661	Dec 20, 2016 (150)
27	HUMAN_LONGEVITY	ss2246942181	Dec 20, 2016 (150)
28	GNOMAD	ss2973843711	Nov 08, 2017 (151)
29	SWEGEN	ss3019223633	Nov 08, 2017 (151)
30	BIOINF_KMB_FNS_UNIBA	ss3028939902	Nov 08, 2017 (151)
31	CSHL	ss3352814182	Nov 08, 2017 (151)
32	ILLUMINA	ss3652642950	Oct 12, 2018 (152)
33	EGCUT_WGS	ss3685720328	Jul 13, 2019 (153)
34	EVA_DECODE	ss3708101072	Jul 13, 2019 (153)
35	ACPOP	ss3743889673	Jul 13, 2019 (153)
36	EVA	ss3759322307	Jul 13, 2019 (153)
37	PACBIO	ss3788815096	Jul 13, 2019 (153)
38	PACBIO	ss3793683086	Jul 13, 2019 (153)
39	PACBIO	ss3798569531	Jul 13, 2019 (153)
40	KHV_HUMAN_GENOMES	ss3822487356	Jul 13, 2019 (153)
41	EVA	ss3825968571	Apr 27, 2020 (154)
42	EVA	ss3835965563	Apr 27, 2020 (154)
43	SGDP_PRJ	ss3890443092	Apr 27, 2020 (154)
44	KRGDB	ss3940826120	Apr 27, 2020 (154)
45	KOGIC	ss3983542796	Apr 27, 2020 (154)
46	KOGIC	ss3983542797	Apr 27, 2020 (154)
47	TOPMED	ss5107546073	Apr 27, 2021 (155)
48	TOPMED	ss5107546074	Apr 27, 2021 (155)
49	TOMMO_GENOMICS	ss5232405255	Apr 27, 2021 (155)
50	TOMMO_GENOMICS	ss5232405256	Apr 27, 2021 (155)
51	1000G_HIGH_COVERAGE	ss5310931412	Oct 16, 2022 (156)
52	EVA	ss5316052887	Oct 16, 2022 (156)
53	EVA	ss5440995555	Oct 16, 2022 (156)
54	HUGCELL_USP	ss5502788313	Oct 16, 2022 (156)
55	EVA	ss5512364649	Oct 16, 2022 (156)
56	1000G_HIGH_COVERAGE	ss5618410164	Oct 16, 2022 (156)
57	SANFORD_IMAGENETICS	ss5664400696	Oct 16, 2022 (156)
58	TOMMO_GENOMICS	ss5793456095	Oct 16, 2022 (156)
59	TOMMO_GENOMICS	ss5793456096	Oct 16, 2022 (156)
60	YY_MCH	ss5818670129	Oct 16, 2022 (156)
61	EVA	ss5822004428	Oct 16, 2022 (156)
62	EVA	ss5853375588	Oct 16, 2022 (156)
63	EVA	ss5881629287	Oct 16, 2022 (156)
64	EVA	ss5959251552	Oct 16, 2022 (156)
65	1000Genomes	NC_000022.10 - 30092695	Oct 12, 2018 (152)
66	1000Genomes_30x	NC_000022.11 - 29696706	Oct 16, 2022 (156)
67	The Avon Longitudinal Study of Parents and Children	NC_000022.10 - 30092695	Oct 12, 2018 (152)
68	Genetic variation in the Estonian population	NC_000022.10 - 30092695	Oct 12, 2018 (152)
69	The Danish reference pan genome	NC_000022.10 - 30092695	Apr 27, 2020 (154)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 568597525 (NC_000022.11:29696705:A:C 1/139298) Row 568597526 (NC_000022.11:29696705:A:G 20332/139246)	-	Apr 27, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 568597525 (NC_000022.11:29696705:A:C 1/139298) Row 568597526 (NC_000022.11:29696705:A:G 20332/139246)	-	Apr 27, 2021 (155)
72	Genome of the Netherlands Release 5	NC_000022.10 - 30092695	Apr 27, 2020 (154)
73	KOREAN population from KRGDB	NC_000022.10 - 30092695	Apr 27, 2020 (154)
74	Korean Genome Project Submission ignored due to conflicting rows: Row 39920797 (NC_000022.11:29696705:A:G 56/1832) Row 39920798 (NC_000022.11:29696705:A:C 2/1832)	-	Apr 27, 2020 (154)
75	Korean Genome Project Submission ignored due to conflicting rows: Row 39920797 (NC_000022.11:29696705:A:G 56/1832) Row 39920798 (NC_000022.11:29696705:A:C 2/1832)	-	Apr 27, 2020 (154)
76	Northern Sweden	NC_000022.10 - 30092695	Jul 13, 2019 (153)
77	Qatari	NC_000022.10 - 30092695	Apr 27, 2020 (154)
78	SGDP_PRJ	NC_000022.10 - 30092695	Apr 27, 2020 (154)
79	Siberian	NC_000022.10 - 30092695	Apr 27, 2020 (154)
80	8.3KJPN Submission ignored due to conflicting rows: Row 90374562 (NC_000022.10:30092694:A:G 373/16760) Row 90374563 (NC_000022.10:30092694:A:C 7/16760)	-	Apr 27, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 90374562 (NC_000022.10:30092694:A:G 373/16760) Row 90374563 (NC_000022.10:30092694:A:C 7/16760)	-	Apr 27, 2021 (155)
82	14KJPN Submission ignored due to conflicting rows: Row 127293199 (NC_000022.11:29696705:A:G 644/28258) Row 127293200 (NC_000022.11:29696705:A:C 10/28258)	-	Oct 16, 2022 (156)
83	14KJPN Submission ignored due to conflicting rows: Row 127293199 (NC_000022.11:29696705:A:G 644/28258) Row 127293200 (NC_000022.11:29696705:A:C 10/28258)	-	Oct 16, 2022 (156)
84	TopMed Submission ignored due to conflicting rows: Row 382655020 (NC_000022.11:29696705:A:C 1/264690) Row 382655021 (NC_000022.11:29696705:A:G 37854/264690)	-	Apr 27, 2021 (155)
85	TopMed Submission ignored due to conflicting rows: Row 382655020 (NC_000022.11:29696705:A:C 1/264690) Row 382655021 (NC_000022.11:29696705:A:G 37854/264690)	-	Apr 27, 2021 (155)
86	UK 10K study - Twins	NC_000022.10 - 30092695	Oct 12, 2018 (152)
87	A Vietnamese Genetic Variation Database	NC_000022.10 - 30092695	Jul 13, 2019 (153)
88	ALFA	NC_000022.11 - 29696706	Apr 27, 2021 (155)
89	ClinVar	RCV000334760.3	Oct 16, 2022 (156)

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
ss5232405256	NC_000022.10:30092694:A:C	NC_000022.11:29696705:A:C	(self)
3974633332, ss3983542797, ss5107546073, ss5793456096	NC_000022.11:29696705:A:C	NC_000022.11:29696705:A:C	(self)
ss114130694, ss169089392, ss171913599, ss255877144, ss484301328, ss1699368690, ss2094922391	NC_000022.9:28422694:A:G	NC_000022.11:29696705:A:G	(self)
80519248, 44535267, 31458576, 5897473, 19846054, 48003514, 17174538, 20907793, 42460072, 11337015, 44535267, 9826762, ss228654923, ss238049785, ss244173493, ss483576649, ss662537823, ss782231768, ss995299595, ss1082621861, ss1366974338, ss1429242422, ss1579732534, ss1639891824, ss1682885857, ss1809766909, ss1938865871, ss1969262390, ss2030204610, ss2095121849, ss2158820661, ss2973843711, ss3019223633, ss3352814182, ss3652642950, ss3685720328, ss3743889673, ss3759322307, ss3788815096, ss3793683086, ss3798569531, ss3825968571, ss3835965563, ss3890443092, ss3940826120, ss5232405255, ss5316052887, ss5440995555, ss5512364649, ss5664400696, ss5822004428, ss5959251552	NC_000022.10:30092694:A:G	NC_000022.11:29696705:A:G	(self)
RCV000334760.3, 105936099, 3974633332, ss2246942181, ss3028939902, ss3708101072, ss3822487356, ss3983542796, ss5107546074, ss5310931412, ss5502788313, ss5618410164, ss5793456095, ss5818670129, ss5853375588, ss5881629287	NC_000022.11:29696705:A:G	NC_000022.11:29696705:A:G	(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 rs73390944

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs73390944