Name: rs10709063
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.

rs10709063

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr20:58342649-58342665 (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: del(A)₅ / del(A)₄ / delAAA / delAA…
del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₇ / dup(A)₉
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.3261 (1633/5008, 1000G)
delAA=0.0739 (285/3854, ALSPAC)
del(A)₅=0.0000 (0/2744, ALFA) (+ 6 more)
delAAA=0.0000 (0/2744, ALFA)
delAA=0.0000 (0/2744, ALFA)
delA=0.0000 (0/2744, ALFA)
dupA=0.0000 (0/2744, ALFA)
dupAA=0.0000 (0/2744, ALFA)
(A)₁₇=0.47 (19/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RAB22A : 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: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	HWEP
Total	Global	2744	AAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	2204	AAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	234	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	2	AAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
African American	Sub	232	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	26	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	16	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	10	AAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	32	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	148	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	14	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	86	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A

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
1000Genomes	Global	Study-wide	5008	(A)₁₇=0.6739	delA=0.3261
1000Genomes	African	Sub	1322	(A)₁₇=0.6513	delA=0.3487
1000Genomes	East Asian	Sub	1008	(A)₁₇=0.7004	delA=0.2996
1000Genomes	Europe	Sub	1006	(A)₁₇=0.7127	delA=0.2873
1000Genomes	South Asian	Sub	978	(A)₁₇=0.626	delA=0.374
1000Genomes	American	Sub	694	(A)₁₇=0.690	delA=0.310
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(A)₁₇=0.9261	delAA=0.0739
Allele Frequency Aggregator	Total	Global	2744	(A)₁₇=1.0000	del(A)₅=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	European	Sub	2204	(A)₁₇=1.0000	del(A)₅=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	African	Sub	234	(A)₁₇=1.000	del(A)₅=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	148	(A)₁₇=1.000	del(A)₅=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Other	Sub	86	(A)₁₇=1.00	del(A)₅=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	32	(A)₁₇=1.00	del(A)₅=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Asian	Sub	26	(A)₁₇=1.00	del(A)₅=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	South Asian	Sub	14	(A)₁₇=1.00	del(A)₅=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
The Danish reference pan genome	Danish	Study-wide	40	(A)₁₇=0.47	delA=0.53

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 20	NC_000020.11:g.58342661_58342665del
GRCh38.p14 chr 20	NC_000020.11:g.58342662_58342665del
GRCh38.p14 chr 20	NC_000020.11:g.58342663_58342665del
GRCh38.p14 chr 20	NC_000020.11:g.58342664_58342665del
GRCh38.p14 chr 20	NC_000020.11:g.58342665del
GRCh38.p14 chr 20	NC_000020.11:g.58342665dup
GRCh38.p14 chr 20	NC_000020.11:g.58342664_58342665dup
GRCh38.p14 chr 20	NC_000020.11:g.58342663_58342665dup
GRCh38.p14 chr 20	NC_000020.11:g.58342659_58342665dup
GRCh38.p14 chr 20	NC_000020.11:g.58342657_58342665dup
GRCh37.p13 chr 20	NC_000020.10:g.56917717_56917721del
GRCh37.p13 chr 20	NC_000020.10:g.56917718_56917721del
GRCh37.p13 chr 20	NC_000020.10:g.56917719_56917721del
GRCh37.p13 chr 20	NC_000020.10:g.56917720_56917721del
GRCh37.p13 chr 20	NC_000020.10:g.56917721del
GRCh37.p13 chr 20	NC_000020.10:g.56917721dup
GRCh37.p13 chr 20	NC_000020.10:g.56917720_56917721dup
GRCh37.p13 chr 20	NC_000020.10:g.56917719_56917721dup
GRCh37.p13 chr 20	NC_000020.10:g.56917715_56917721dup
GRCh37.p13 chr 20	NC_000020.10:g.56917713_56917721dup

Gene: RAB22A, RAB22A, member RAS oncogene family (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RAB22A transcript	NM_020673.3:c.117-1057_11… NM_020673.3:c.117-1057_117-1053del	N/A	Intron 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	(A)₁₇=	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₇	dup(A)₉
GRCh38.p14 chr 20	NC_000020.11:g.58342649_58342665=	NC_000020.11:g.58342661_58342665del	NC_000020.11:g.58342662_58342665del	NC_000020.11:g.58342663_58342665del	NC_000020.11:g.58342664_58342665del	NC_000020.11:g.58342665del	NC_000020.11:g.58342665dup	NC_000020.11:g.58342664_58342665dup	NC_000020.11:g.58342663_58342665dup	NC_000020.11:g.58342659_58342665dup	NC_000020.11:g.58342657_58342665dup
GRCh37.p13 chr 20	NC_000020.10:g.56917705_56917721=	NC_000020.10:g.56917717_56917721del	NC_000020.10:g.56917718_56917721del	NC_000020.10:g.56917719_56917721del	NC_000020.10:g.56917720_56917721del	NC_000020.10:g.56917721del	NC_000020.10:g.56917721dup	NC_000020.10:g.56917720_56917721dup	NC_000020.10:g.56917719_56917721dup	NC_000020.10:g.56917715_56917721dup	NC_000020.10:g.56917713_56917721dup
RAB22A transcript	NM_020673.2:c.117-1069=	NM_020673.2:c.117-1057_117-1053del	NM_020673.2:c.117-1056_117-1053del	NM_020673.2:c.117-1055_117-1053del	NM_020673.2:c.117-1054_117-1053del	NM_020673.2:c.117-1053del	NM_020673.2:c.117-1053dup	NM_020673.2:c.117-1054_117-1053dup	NM_020673.2:c.117-1055_117-1053dup	NM_020673.2:c.117-1059_117-1053dup	NM_020673.2:c.117-1061_117-1053dup
RAB22A transcript	NM_020673.3:c.117-1069=	NM_020673.3:c.117-1057_117-1053del	NM_020673.3:c.117-1056_117-1053del	NM_020673.3:c.117-1055_117-1053del	NM_020673.3:c.117-1054_117-1053del	NM_020673.3:c.117-1053del	NM_020673.3:c.117-1053dup	NM_020673.3:c.117-1054_117-1053dup	NM_020673.3:c.117-1055_117-1053dup	NM_020673.3:c.117-1059_117-1053dup	NM_020673.3:c.117-1061_117-1053dup
RAB22A transcript variant X1	XM_005260469.1:c.117-1069=	XM_005260469.1:c.117-1057_117-1053del	XM_005260469.1:c.117-1056_117-1053del	XM_005260469.1:c.117-1055_117-1053del	XM_005260469.1:c.117-1054_117-1053del	XM_005260469.1:c.117-1053del	XM_005260469.1:c.117-1053dup	XM_005260469.1:c.117-1054_117-1053dup	XM_005260469.1:c.117-1055_117-1053dup	XM_005260469.1:c.117-1059_117-1053dup	XM_005260469.1:c.117-1061_117-1053dup

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#.

61 SubSNP, 26 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	DEVINE_LAB	ss15147233	Mar 15, 2016 (147)
2	ABI	ss41375353	Dec 03, 2013 (138)
3	HGSV	ss81554722	Sep 08, 2015 (146)
4	HUMANGENOME_JCVI	ss96247206	Dec 05, 2013 (138)
5	BUSHMAN	ss193620247	Jul 04, 2010 (137)
6	GMI	ss289418780	May 04, 2012 (138)
7	PJP	ss295055831	May 09, 2011 (137)
8	PJP	ss295055832	May 09, 2011 (138)
9	SSMP	ss664485688	Apr 01, 2015 (144)
10	BILGI_BIOE	ss666750616	Apr 25, 2013 (138)
11	1000GENOMES	ss1378553839	Aug 21, 2014 (142)
12	EVA_GENOME_DK	ss1575727225	Apr 01, 2015 (144)
13	EVA_UK10K_ALSPAC	ss1709411863	Apr 01, 2015 (144)
14	EVA_UK10K_TWINSUK	ss1709412119	Apr 01, 2015 (144)
15	EVA_UK10K_ALSPAC	ss1710820838	Apr 01, 2015 (144)
16	EVA_UK10K_TWINSUK	ss1710820845	Apr 01, 2015 (144)
17	HAMMER_LAB	ss1809565559	Sep 08, 2015 (146)
18	HAMMER_LAB	ss1809565560	Sep 08, 2015 (146)
19	SYSTEMSBIOZJU	ss2629479600	Nov 08, 2017 (151)
20	SWEGEN	ss3018405575	Nov 08, 2017 (151)
21	MCHAISSO	ss3064861154	Nov 08, 2017 (151)
22	MCHAISSO	ss3065825518	Nov 08, 2017 (151)
23	URBANLAB	ss3651047645	Oct 12, 2018 (152)
24	EVA_DECODE	ss3707224437	Jul 13, 2019 (153)
25	EVA_DECODE	ss3707224438	Jul 13, 2019 (153)
26	EVA_DECODE	ss3707224439	Jul 13, 2019 (153)
27	EVA_DECODE	ss3707224440	Jul 13, 2019 (153)
28	EVA_DECODE	ss3707224441	Jul 13, 2019 (153)
29	ACPOP	ss3743513875	Jul 13, 2019 (153)
30	ACPOP	ss3743513876	Jul 13, 2019 (153)
31	ACPOP	ss3743513877	Jul 13, 2019 (153)
32	PACBIO	ss3788684688	Jul 13, 2019 (153)
33	KHV_HUMAN_GENOMES	ss3821971146	Jul 13, 2019 (153)
34	EVA	ss3835743034	Apr 27, 2020 (154)
35	EVA	ss3847009370	Apr 27, 2020 (154)
36	KOGIC	ss3982559293	Apr 27, 2020 (154)
37	KOGIC	ss3982559294	Apr 27, 2020 (154)
38	KOGIC	ss3982559295	Apr 27, 2020 (154)
39	GNOMAD	ss4355758872	Apr 26, 2021 (155)
40	GNOMAD	ss4355758873	Apr 26, 2021 (155)
41	GNOMAD	ss4355758874	Apr 26, 2021 (155)
42	GNOMAD	ss4355758875	Apr 26, 2021 (155)
43	GNOMAD	ss4355758876	Apr 26, 2021 (155)
44	GNOMAD	ss4355758877	Apr 26, 2021 (155)
45	GNOMAD	ss4355758878	Apr 26, 2021 (155)
46	GNOMAD	ss4355758879	Apr 26, 2021 (155)
47	GNOMAD	ss4355758880	Apr 26, 2021 (155)
48	GNOMAD	ss4355758881	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5230274057	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5230274058	Apr 26, 2021 (155)
51	1000G_HIGH_COVERAGE	ss5309285756	Oct 13, 2022 (156)
52	1000G_HIGH_COVERAGE	ss5309285757	Oct 13, 2022 (156)
53	1000G_HIGH_COVERAGE	ss5309285758	Oct 13, 2022 (156)
54	HUGCELL_USP	ss5501518906	Oct 13, 2022 (156)
55	HUGCELL_USP	ss5501518907	Oct 13, 2022 (156)
56	HUGCELL_USP	ss5501518908	Oct 13, 2022 (156)
57	TOMMO_GENOMICS	ss5790269633	Oct 13, 2022 (156)
58	TOMMO_GENOMICS	ss5790269634	Oct 13, 2022 (156)
59	EVA	ss5845883391	Oct 13, 2022 (156)
60	EVA	ss5845883392	Oct 13, 2022 (156)
61	EVA	ss5853200349	Oct 13, 2022 (156)
62	1000Genomes	NC_000020.10 - 56917705	Oct 12, 2018 (152)
63	The Avon Longitudinal Study of Parents and Children	NC_000020.10 - 56917705	Oct 12, 2018 (152)
64	The Danish reference pan genome	NC_000020.10 - 56917705	Apr 27, 2020 (154)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 555778682 (NC_000020.11:58342648::A 1344/113860) Row 555778683 (NC_000020.11:58342648::AA 2/113888) Row 555778684 (NC_000020.11:58342648::AAA 1/113890)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 555778682 (NC_000020.11:58342648::A 1344/113860) Row 555778683 (NC_000020.11:58342648::AA 2/113888) Row 555778684 (NC_000020.11:58342648::AAA 1/113890)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 555778682 (NC_000020.11:58342648::A 1344/113860) Row 555778683 (NC_000020.11:58342648::AA 2/113888) Row 555778684 (NC_000020.11:58342648::AAA 1/113890)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 555778682 (NC_000020.11:58342648::A 1344/113860) Row 555778683 (NC_000020.11:58342648::AA 2/113888) Row 555778684 (NC_000020.11:58342648::AAA 1/113890)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 555778682 (NC_000020.11:58342648::A 1344/113860) Row 555778683 (NC_000020.11:58342648::AA 2/113888) Row 555778684 (NC_000020.11:58342648::AAA 1/113890)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 555778682 (NC_000020.11:58342648::A 1344/113860) Row 555778683 (NC_000020.11:58342648::AA 2/113888) Row 555778684 (NC_000020.11:58342648::AAA 1/113890)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 555778682 (NC_000020.11:58342648::A 1344/113860) Row 555778683 (NC_000020.11:58342648::AA 2/113888) Row 555778684 (NC_000020.11:58342648::AAA 1/113890)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 555778682 (NC_000020.11:58342648::A 1344/113860) Row 555778683 (NC_000020.11:58342648::AA 2/113888) Row 555778684 (NC_000020.11:58342648::AAA 1/113890)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 555778682 (NC_000020.11:58342648::A 1344/113860) Row 555778683 (NC_000020.11:58342648::AA 2/113888) Row 555778684 (NC_000020.11:58342648::AAA 1/113890)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 555778682 (NC_000020.11:58342648::A 1344/113860) Row 555778683 (NC_000020.11:58342648::AA 2/113888) Row 555778684 (NC_000020.11:58342648::AAA 1/113890)...	-	Apr 26, 2021 (155)
75	Korean Genome Project Submission ignored due to conflicting rows: Row 38937294 (NC_000020.11:58342648:AA: 42/1826) Row 38937295 (NC_000020.11:58342649:A: 729/1826) Row 38937296 (NC_000020.11:58342650::A 75/1826)	-	Apr 27, 2020 (154)
76	Korean Genome Project Submission ignored due to conflicting rows: Row 38937294 (NC_000020.11:58342648:AA: 42/1826) Row 38937295 (NC_000020.11:58342649:A: 729/1826) Row 38937296 (NC_000020.11:58342650::A 75/1826)	-	Apr 27, 2020 (154)
77	Korean Genome Project Submission ignored due to conflicting rows: Row 38937294 (NC_000020.11:58342648:AA: 42/1826) Row 38937295 (NC_000020.11:58342649:A: 729/1826) Row 38937296 (NC_000020.11:58342650::A 75/1826)	-	Apr 27, 2020 (154)
78	Northern Sweden Submission ignored due to conflicting rows: Row 16798740 (NC_000020.10:56917704:A: 223/560) Row 16798741 (NC_000020.10:56917704::A 7/560) Row 16798742 (NC_000020.10:56917704:AA: 6/560)	-	Jul 13, 2019 (153)
79	Northern Sweden Submission ignored due to conflicting rows: Row 16798740 (NC_000020.10:56917704:A: 223/560) Row 16798741 (NC_000020.10:56917704::A 7/560) Row 16798742 (NC_000020.10:56917704:AA: 6/560)	-	Jul 13, 2019 (153)
80	Northern Sweden Submission ignored due to conflicting rows: Row 16798740 (NC_000020.10:56917704:A: 223/560) Row 16798741 (NC_000020.10:56917704::A 7/560) Row 16798742 (NC_000020.10:56917704:AA: 6/560)	-	Jul 13, 2019 (153)
81	8.3KJPN Submission ignored due to conflicting rows: Row 88243364 (NC_000020.10:56917704:A: 6003/16752) Row 88243365 (NC_000020.10:56917704::A 116/16752)	-	Apr 26, 2021 (155)
82	8.3KJPN Submission ignored due to conflicting rows: Row 88243364 (NC_000020.10:56917704:A: 6003/16752) Row 88243365 (NC_000020.10:56917704::A 116/16752)	-	Apr 26, 2021 (155)
83	14KJPN Submission ignored due to conflicting rows: Row 124106737 (NC_000020.11:58342648:A: 10077/28258) Row 124106738 (NC_000020.11:58342648::A 207/28258)	-	Oct 13, 2022 (156)
84	14KJPN Submission ignored due to conflicting rows: Row 124106737 (NC_000020.11:58342648:A: 10077/28258) Row 124106738 (NC_000020.11:58342648::A 207/28258)	-	Oct 13, 2022 (156)
85	UK 10K study - Twins Submission ignored due to conflicting rows: Row 43631314 (NC_000020.10:56917705:A: 1742/3708) Row 43631315 (NC_000020.10:56917704:AA: 263/3708)	-	Apr 27, 2020 (154)
86	UK 10K study - Twins	-	Oct 12, 2018 (152)
87	ALFA	NC_000020.11 - 58342649	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)
rs11478886	Apr 25, 2013 (138)
rs33924102	May 23, 2006 (127)
rs60285884	May 25, 2008 (130)
rs71828900	May 04, 2012 (137)
rs112580245	Oct 18, 2011 (136)
rs199696276	May 11, 2012 (137)
rs371178153	May 13, 2013 (138)
rs869053768	Jul 19, 2016 (147)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4355758881	NC_000020.11:58342648:AAAAA:	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
9726068682	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3707224441, ss4355758880	NC_000020.11:58342648:AAAA:	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4355758879	NC_000020.11:58342648:AAA:	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
9726068682	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3707224440	NC_000020.11:58342649:AAA:	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
43631315, ss1709411863, ss1709412119, ss1809565560, ss3018405575, ss3743513877, ss5845883392	NC_000020.10:56917704:AA:	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3982559293, ss4355758878, ss5309285756, ss5501518906	NC_000020.11:58342648:AA:	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
9726068682	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3707224439	NC_000020.11:58342650:AA:	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss289418780, ss295055831	NC_000020.9:56351110:A:	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss81554722, ss295055832	NC_000020.9:56351126:A:	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
78800808, 766624, ss664485688, ss666750616, ss1378553839, ss1575727225, ss1809565559, ss2629479600, ss3743513875, ss3788684688, ss3835743034, ss5230274057, ss5845883391	NC_000020.10:56917704:A:	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss1710820838, ss1710820845	NC_000020.10:56917705:A:	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3064861154, ss3065825518, ss3651047645, ss3821971146, ss3847009370, ss4355758877, ss5309285757, ss5501518907, ss5790269633, ss5853200349	NC_000020.11:58342648:A:	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
9726068682	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3982559294	NC_000020.11:58342649:A:	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3707224438	NC_000020.11:58342651:A:	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss15147233	NT_011362.10:27113796:A:	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss41375353, ss96247206	NT_011362.10:27113812:A:	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss193620247	NT_011362.11:27291140:A:	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3743513876, ss5230274058	NC_000020.10:56917704::A	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4355758872, ss5309285758, ss5501518908, ss5790269634	NC_000020.11:58342648::A	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
9726068682	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3982559295	NC_000020.11:58342650::A	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3707224437	NC_000020.11:58342652::A	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4355758873	NC_000020.11:58342648::AA	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
9726068682	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4355758874	NC_000020.11:58342648::AAA	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4355758875	NC_000020.11:58342648::AAAAAAA	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4355758876	NC_000020.11:58342648::AAAAAAAAA	NC_000020.11:58342648:AAAAAAAAAAAA… NC_000020.11:58342648:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs10709063

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

rs10709063