Name: rs79213522
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.

rs79213522

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr20:19711133-19711147 (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(CA)₃ / delCACA / delCA / dupCA…
del(CA)₃ / delCACA / delCA / dupCA / dupCACA / dup(CA)₃
Variation Type: Indel Insertion and Deletion
Frequency: dupCA=0.4735 (2665/5628, ALFA)
(AC)₇A=0.0655 (120/1832, Korea1K)
(AC)₇A=0.369 (368/998, GoNL) (+ 1 more)
(AC)₇A=0.390 (234/600, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SLC24A3 : 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	Alt HMOZ	HTRZ	HWEP
Total	Global	5628	ACACACACACACACA=0.5265	ACACACACA=0.0000, ACACACACACA=0.0000, ACACACACACACA=0.0000, ACACACACACACACACA=0.4735, ACACACACACACACACACA=0.0000, ACACACACACACACACACACA=0.0000	0.343639	0.290689	0.365672	32
European	Sub	5270	ACACACACACACACA=0.4951	ACACACACA=0.0000, ACACACACACA=0.0000, ACACACACACACA=0.0000, ACACACACACACACACA=0.5049, ACACACACACACACACACA=0.0000, ACACACACACACACACACACA=0.0000	0.30019	0.310057	0.389753	32
African	Sub	264	ACACACACACACACA=1.000	ACACACACA=0.000, ACACACACACA=0.000, ACACACACACACA=0.000, ACACACACACACACACA=0.000, ACACACACACACACACACA=0.000, ACACACACACACACACACACA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	6	ACACACACACACACA=1.0	ACACACACA=0.0, ACACACACACA=0.0, ACACACACACACA=0.0, ACACACACACACACACA=0.0, ACACACACACACACACACA=0.0, ACACACACACACACACACACA=0.0	1.0	0.0	0.0	N/A
African American	Sub	258	ACACACACACACACA=1.000	ACACACACA=0.000, ACACACACACA=0.000, ACACACACACACA=0.000, ACACACACACACACACA=0.000, ACACACACACACACACACA=0.000, ACACACACACACACACACACA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	0	ACACACACACACACA=0	ACACACACA=0, ACACACACACA=0, ACACACACACACA=0, ACACACACACACACACA=0, ACACACACACACACACACA=0, ACACACACACACACACACACA=0	0	0	0	N/A
East Asian	Sub	0	ACACACACACACACA=0	ACACACACA=0, ACACACACACA=0, ACACACACACACA=0, ACACACACACACACACA=0, ACACACACACACACACACA=0, ACACACACACACACACACACA=0	0	0	0	N/A
Other Asian	Sub	0	ACACACACACACACA=0	ACACACACA=0, ACACACACACA=0, ACACACACACACA=0, ACACACACACACACACA=0, ACACACACACACACACACA=0, ACACACACACACACACACACA=0	0	0	0	N/A
Latin American 1	Sub	14	ACACACACACACACA=1.00	ACACACACA=0.00, ACACACACACA=0.00, ACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	26	ACACACACACACACA=1.00	ACACACACA=0.00, ACACACACACA=0.00, ACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	2	ACACACACACACACA=1.0	ACACACACA=0.0, ACACACACACA=0.0, ACACACACACACA=0.0, ACACACACACACACACA=0.0, ACACACACACACACACACA=0.0, ACACACACACACACACACACA=0.0	1.0	0.0	0.0	N/A
Other	Sub	52	ACACACACACACACA=0.92	ACACACACA=0.00, ACACACACACA=0.00, ACACACACACACA=0.00, ACACACACACACACACA=0.08, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00	0.884615	0.038462	0.076923	3

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	5628	(AC)₇A=0.5265	del(CA)₃=0.0000, delCACA=0.0000, delCA=0.0000, dupCA=0.4735, dupCACA=0.0000, dup(CA)₃=0.0000
Allele Frequency Aggregator	European	Sub	5270	(AC)₇A=0.4951	del(CA)₃=0.0000, delCACA=0.0000, delCA=0.0000, dupCA=0.5049, dupCACA=0.0000, dup(CA)₃=0.0000
Allele Frequency Aggregator	African	Sub	264	(AC)₇A=1.000	del(CA)₃=0.000, delCACA=0.000, delCA=0.000, dupCA=0.000, dupCACA=0.000, dup(CA)₃=0.000
Allele Frequency Aggregator	Other	Sub	52	(AC)₇A=0.92	del(CA)₃=0.00, delCACA=0.00, delCA=0.00, dupCA=0.08, dupCACA=0.00, dup(CA)₃=0.00
Allele Frequency Aggregator	Latin American 2	Sub	26	(AC)₇A=1.00	del(CA)₃=0.00, delCACA=0.00, delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00
Allele Frequency Aggregator	Latin American 1	Sub	14	(AC)₇A=1.00	del(CA)₃=0.00, delCACA=0.00, delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00
Allele Frequency Aggregator	South Asian	Sub	2	(AC)₇A=1.0	del(CA)₃=0.0, delCACA=0.0, delCA=0.0, dupCA=0.0, dupCACA=0.0, dup(CA)₃=0.0
Allele Frequency Aggregator	Asian	Sub	0	(AC)₇A=0	del(CA)₃=0, delCACA=0, delCA=0, dupCA=0, dupCACA=0, dup(CA)₃=0
Korean Genome Project	KOREAN	Study-wide	1832	- No frequency provided	dupCA=0.9345
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	- No frequency provided	dupCA=0.631
Northern Sweden	ACPOP	Study-wide	600	- No frequency provided	dupCA=0.610

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.19711134CA[4]
GRCh38.p14 chr 20	NC_000020.11:g.19711134CA[5]
GRCh38.p14 chr 20	NC_000020.11:g.19711134CA[6]
GRCh38.p14 chr 20	NC_000020.11:g.19711134CA[8]
GRCh38.p14 chr 20	NC_000020.11:g.19711134CA[9]
GRCh38.p14 chr 20	NC_000020.11:g.19711134CA[10]
GRCh37.p13 chr 20	NC_000020.10:g.19691778CA[4]
GRCh37.p13 chr 20	NC_000020.10:g.19691778CA[5]
GRCh37.p13 chr 20	NC_000020.10:g.19691778CA[6]
GRCh37.p13 chr 20	NC_000020.10:g.19691778CA[8]
GRCh37.p13 chr 20	NC_000020.10:g.19691778CA[9]
GRCh37.p13 chr 20	NC_000020.10:g.19691778CA[10]

Gene: SLC24A3, solute carrier family 24 member 3 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SLC24A3 transcript	NM_020689.4:c.1720-6395AC… NM_020689.4:c.1720-6395AC[4]	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	(AC)₇A=	del(CA)₃	delCACA	delCA	dupCA	dupCACA	dup(CA)₃
GRCh38.p14 chr 20	NC_000020.11:g.19711133_19711147=	NC_000020.11:g.19711134CA[4]	NC_000020.11:g.19711134CA[5]	NC_000020.11:g.19711134CA[6]	NC_000020.11:g.19711134CA[8]	NC_000020.11:g.19711134CA[9]	NC_000020.11:g.19711134CA[10]
GRCh37.p13 chr 20	NC_000020.10:g.19691777_19691791=	NC_000020.10:g.19691778CA[4]	NC_000020.10:g.19691778CA[5]	NC_000020.10:g.19691778CA[6]	NC_000020.10:g.19691778CA[8]	NC_000020.10:g.19691778CA[9]	NC_000020.10:g.19691778CA[10]
SLC24A3 transcript	NM_020689.3:c.1720-6395=	NM_020689.3:c.1720-6395AC[4]	NM_020689.3:c.1720-6395AC[5]	NM_020689.3:c.1720-6395AC[6]	NM_020689.3:c.1720-6395AC[8]	NM_020689.3:c.1720-6395AC[9]	NM_020689.3:c.1720-6395AC[10]
SLC24A3 transcript	NM_020689.4:c.1720-6395=	NM_020689.4:c.1720-6395AC[4]	NM_020689.4:c.1720-6395AC[5]	NM_020689.4:c.1720-6395AC[6]	NM_020689.4:c.1720-6395AC[8]	NM_020689.4:c.1720-6395AC[9]	NM_020689.4:c.1720-6395AC[10]

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#.

53 SubSNP, 15 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss4290780	Dec 03, 2013 (138)
2	HGSV	ss81544630	Dec 04, 2013 (138)
3	HUMANGENOME_JCVI	ss95737715	Oct 12, 2018 (152)
4	GMI	ss155791083	Dec 01, 2009 (131)
5	BUSHMAN	ss193606727	Jul 04, 2010 (132)
6	BL	ss256193834	May 09, 2011 (135)
7	GMI	ss288534494	Dec 06, 2013 (138)
8	GMI	ss289405611	May 04, 2012 (137)
9	GMI	ss289405612	Oct 12, 2018 (152)
10	SSMP	ss664466008	Apr 01, 2015 (144)
11	BILGI_BIOE	ss666742282	Apr 25, 2013 (138)
12	EVA-GONL	ss994614403	Aug 21, 2014 (142)
13	DDI	ss1536904768	Apr 01, 2015 (144)
14	EVA_UK10K_ALSPAC	ss1709320610	Jan 10, 2018 (151)
15	EVA_UK10K_TWINSUK	ss1709321046	Jan 10, 2018 (151)
16	EVA_UK10K_ALSPAC	ss1710808757	Apr 01, 2015 (144)
17	EVA_UK10K_TWINSUK	ss1710808758	Apr 01, 2015 (144)
18	HAMMER_LAB	ss1809453364	Sep 08, 2015 (146)
19	JJLAB	ss2031425787	Sep 14, 2016 (149)
20	SYSTEMSBIOZJU	ss2629418208	Nov 08, 2017 (151)
21	SWEGEN	ss3017977687	Nov 08, 2017 (151)
22	MCHAISSO	ss3063992623	Nov 08, 2017 (151)
23	MCHAISSO	ss3065811048	Nov 08, 2017 (151)
24	URBANLAB	ss3650987339	Oct 12, 2018 (152)
25	EVA_DECODE	ss3706694946	Jul 13, 2019 (153)
26	EVA_DECODE	ss3706694947	Jul 13, 2019 (153)
27	EVA_DECODE	ss3706694948	Jul 13, 2019 (153)
28	ACPOP	ss3743310911	Jul 13, 2019 (153)
29	PACBIO	ss3788618431	Jul 13, 2019 (153)
30	PACBIO	ss3793516117	Jul 13, 2019 (153)
31	PACBIO	ss3798403290	Jul 13, 2019 (153)
32	KHV_HUMAN_GENOMES	ss3821679472	Jul 13, 2019 (153)
33	EVA	ss3835624910	Apr 27, 2020 (154)
34	EVA	ss3841438776	Apr 27, 2020 (154)
35	EVA	ss3846946867	Apr 27, 2020 (154)
36	KOGIC	ss3981948020	Apr 27, 2020 (154)
37	GNOMAD	ss4336206140	Apr 26, 2021 (155)
38	GNOMAD	ss4336206141	Apr 26, 2021 (155)
39	GNOMAD	ss4336206143	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5229140264	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5229140265	Apr 26, 2021 (155)
42	1000G_HIGH_COVERAGE	ss5308318692	Oct 13, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5308318693	Oct 13, 2022 (156)
44	HUGCELL_USP	ss5500699487	Oct 13, 2022 (156)
45	SANFORD_IMAGENETICS	ss5663000045	Oct 13, 2022 (156)
46	TOMMO_GENOMICS	ss5788210866	Oct 13, 2022 (156)
47	TOMMO_GENOMICS	ss5788210867	Oct 13, 2022 (156)
48	YY_MCH	ss5817877097	Oct 13, 2022 (156)
49	EVA	ss5845540326	Oct 13, 2022 (156)
50	EVA	ss5845540327	Oct 13, 2022 (156)
51	EVA	ss5853099468	Oct 13, 2022 (156)
52	EVA	ss5922947561	Oct 13, 2022 (156)
53	EVA	ss5981080392	Oct 13, 2022 (156)
54	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 43067178 (NC_000020.10:19691776::AC 2492/3854) Row 43067179 (NC_000020.10:19691776:AC: 16/3854)	-	Oct 12, 2018 (152)
55	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 43067178 (NC_000020.10:19691776::AC 2492/3854) Row 43067179 (NC_000020.10:19691776:AC: 16/3854)	-	Oct 12, 2018 (152)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 548395296 (NC_000020.11:19711132::AC 94586/138250) Row 548395297 (NC_000020.11:19711132::ACAC 27/138386) Row 548395299 (NC_000020.11:19711132:AC: 5/138384)	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 548395296 (NC_000020.11:19711132::AC 94586/138250) Row 548395297 (NC_000020.11:19711132::ACAC 27/138386) Row 548395299 (NC_000020.11:19711132:AC: 5/138384)	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 548395296 (NC_000020.11:19711132::AC 94586/138250) Row 548395297 (NC_000020.11:19711132::ACAC 27/138386) Row 548395299 (NC_000020.11:19711132:AC: 5/138384)	-	Apr 26, 2021 (155)
59	Genome of the Netherlands Release 5	NC_000020.10 - 19691777	Apr 27, 2020 (154)
60	Korean Genome Project	NC_000020.11 - 19711133	Apr 27, 2020 (154)
61	Northern Sweden	NC_000020.10 - 19691777	Jul 13, 2019 (153)
62	8.3KJPN Submission ignored due to conflicting rows: Row 87109571 (NC_000020.10:19691776::AC 16006/16760) Row 87109572 (NC_000020.10:19691776::ACAC 31/16760)	-	Apr 26, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 87109571 (NC_000020.10:19691776::AC 16006/16760) Row 87109572 (NC_000020.10:19691776::ACAC 31/16760)	-	Apr 26, 2021 (155)
64	14KJPN Submission ignored due to conflicting rows: Row 122047970 (NC_000020.11:19711132::AC 27004/28250) Row 122047971 (NC_000020.11:19711132::ACAC 49/28250)	-	Oct 13, 2022 (156)
65	14KJPN Submission ignored due to conflicting rows: Row 122047970 (NC_000020.11:19711132::AC 27004/28250) Row 122047971 (NC_000020.11:19711132::ACAC 49/28250)	-	Oct 13, 2022 (156)
66	UK 10K study - Twins Submission ignored due to conflicting rows: Row 43067178 (NC_000020.10:19691776::AC 2386/3708) Row 43067179 (NC_000020.10:19691776:AC: 10/3708)	-	Oct 12, 2018 (152)
67	UK 10K study - Twins Submission ignored due to conflicting rows: Row 43067178 (NC_000020.10:19691776::AC 2386/3708) Row 43067179 (NC_000020.10:19691776:AC: 10/3708)	-	Oct 12, 2018 (152)
68	ALFA	NC_000020.11 - 19711133	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)
rs143005873	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
2976166449	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACA	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACA	(self)
ss3706694948	NC_000020.11:19711132:ACAC:	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACACA	(self)
2976166449	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACACA	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACACA	(self)
ss1709320610, ss1709321046, ss5845540327	NC_000020.10:19691776:AC:	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACACACA	(self)
ss4336206143	NC_000020.11:19711132:AC:	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACACACA	(self)
2976166449	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACACACA	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACACACA	(self)
ss3706694947	NC_000020.11:19711134:AC:	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACACACA	(self)
ss256193834, ss289405611	NC_000020.9:19639776::AC	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACACACACACA	(self)
ss289405612	NC_000020.9:19639791::CA	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACACACACACA	(self)
19191174, 16595776, ss664466008, ss666742282, ss994614403, ss1536904768, ss1809453364, ss2031425787, ss2629418208, ss3017977687, ss3743310911, ss3788618431, ss3793516117, ss3798403290, ss3835624910, ss3841438776, ss5229140264, ss5663000045, ss5845540326, ss5981080392	NC_000020.10:19691776::AC	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACACACACACA	(self)
ss1710808757, ss1710808758	NC_000020.10:19691778::AC	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACACACACACA	(self)
38326021, ss3063992623, ss3065811048, ss3650987339, ss3821679472, ss3846946867, ss3981948020, ss4336206140, ss5308318692, ss5500699487, ss5788210866, ss5817877097, ss5853099468, ss5922947561	NC_000020.11:19711132::AC	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACACACACACA	(self)
2976166449	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACACACACACA	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACACACACACA	(self)
ss3706694946	NC_000020.11:19711136::AC	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACACACACACA	(self)
ss155791083	NT_011387.8:19631776::AC	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACACACACACA	(self)
ss4290780, ss81544630, ss95737715, ss288534494	NT_011387.8:19631791::CA	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACACACACACA	(self)
ss193606727	NT_011387.9:19651132::AC	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACACACACACA	(self)
ss5229140265	NC_000020.10:19691776::ACAC	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACACACACACACA	(self)
ss4336206141, ss5308318693, ss5788210867	NC_000020.11:19711132::ACAC	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACACACACACACA	(self)
2976166449	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACACACACACACA	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACACACACACACA	(self)
2976166449	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACACACACACACACA	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACACACACACACACA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3356644442	NC_000020.11:19711132::ACACAC	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACACACACACACACA
ss3356644445	NC_000020.11:19711132:ACACAC:	NC_000020.11:19711132:ACACACACACAC… NC_000020.11:19711132:ACACACACACACACA:ACACACACA

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

No publications for rs79213522

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

rs79213522