Name: rs113383928
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.

rs113383928

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:32199369-32199376 (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: delG / dupG / dupGG / dupGGG
Variation Type: Indel Insertion and Deletion
Frequency: dupGGG=0.000004 (1/264690, TOPMED)
delG=0.03669 (447/12184, ALFA)
dupG=0.0395 (198/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CCDC28B : 5 Prime UTR 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	12184	GGGGGGGG=0.93048	GGGGGGG=0.03669, GGGGGGGGG=0.03283, GGGGGGGGGG=0.00000, GGGGGGGGGGG=0.00000	0.932598	0.002801	0.064601	7
European	Sub	9726	GGGGGGGG=0.9129	GGGGGGG=0.0460, GGGGGGGGG=0.0411, GGGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000	0.91412	0.003569	0.082311	4
African	Sub	1562	GGGGGGGG=1.0000	GGGGGGG=0.0000, GGGGGGGGG=0.0000, GGGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	58	GGGGGGGG=1.00	GGGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGG=0.00	1.0	0.0	0.0	N/A
African American	Sub	1504	GGGGGGGG=1.0000	GGGGGGG=0.0000, GGGGGGGGG=0.0000, GGGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	50	GGGGGGGG=1.00	GGGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGG=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	36	GGGGGGGG=1.00	GGGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGG=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	14	GGGGGGGG=1.00	GGGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGG=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	90	GGGGGGGG=1.00	GGGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGG=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	402	GGGGGGGG=1.000	GGGGGGG=0.000, GGGGGGGGG=0.000, GGGGGGGGGG=0.000, GGGGGGGGGGG=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	50	GGGGGGGG=1.00	GGGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGG=0.00	1.0	0.0	0.0	N/A
Other	Sub	304	GGGGGGGG=1.000	GGGGGGG=0.000, GGGGGGGGG=0.000, GGGGGGGGGG=0.000, GGGGGGGGGGG=0.000	1.0	0.0	0.0	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
TopMed	Global	Study-wide	264690	- No frequency provided	dupGGG=0.000004
Allele Frequency Aggregator	Total	Global	12184	(G)₈=0.93048	delG=0.03669, dupG=0.03283, dupGG=0.00000, dupGGG=0.00000
Allele Frequency Aggregator	European	Sub	9726	(G)₈=0.9129	delG=0.0460, dupG=0.0411, dupGG=0.0000, dupGGG=0.0000
Allele Frequency Aggregator	African	Sub	1562	(G)₈=1.0000	delG=0.0000, dupG=0.0000, dupGG=0.0000, dupGGG=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	402	(G)₈=1.000	delG=0.000, dupG=0.000, dupGG=0.000, dupGGG=0.000
Allele Frequency Aggregator	Other	Sub	304	(G)₈=1.000	delG=0.000, dupG=0.000, dupGG=0.000, dupGGG=0.000
Allele Frequency Aggregator	Latin American 1	Sub	90	(G)₈=1.00	delG=0.00, dupG=0.00, dupGG=0.00, dupGGG=0.00
Allele Frequency Aggregator	South Asian	Sub	50	(G)₈=1.00	delG=0.00, dupG=0.00, dupGG=0.00, dupGGG=0.00
Allele Frequency Aggregator	Asian	Sub	50	(G)₈=1.00	delG=0.00, dupG=0.00, dupGG=0.00, dupGGG=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupG=0.0395
1000Genomes	African	Sub	1322	- No frequency provided	dupG=0.0182
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupG=0.0040
1000Genomes	Europe	Sub	1006	- No frequency provided	dupG=0.1133
1000Genomes	South Asian	Sub	978	- No frequency provided	dupG=0.014
1000Genomes	American	Sub	694	- No frequency provided	dupG=0.061

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 1	NC_000001.11:g.32199376del
GRCh38.p14 chr 1	NC_000001.11:g.32199376dup
GRCh38.p14 chr 1	NC_000001.11:g.32199375_32199376dup
GRCh38.p14 chr 1	NC_000001.11:g.32199374_32199376dup
GRCh37.p13 chr 1	NC_000001.10:g.32664977del
GRCh37.p13 chr 1	NC_000001.10:g.32664977dup
GRCh37.p13 chr 1	NC_000001.10:g.32664976_32664977dup
GRCh37.p13 chr 1	NC_000001.10:g.32664975_32664977dup
CCDC28B RefSeqGene	NG_012178.1:g.3776del
CCDC28B RefSeqGene	NG_012178.1:g.3776dup
CCDC28B RefSeqGene	NG_012178.1:g.3775_3776dup
CCDC28B RefSeqGene	NG_012178.1:g.3774_3776dup

Gene: CCDC28B, coiled-coil domain containing 28B (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CCDC28B transcript variant 1	NM_001301011.2:c.	N/A	Genic Upstream Transcript Variant
CCDC28B transcript variant 2	NM_024296.5:c.	N/A	Genic Upstream Transcript Variant
CCDC28B transcript variant X1	XM_047430215.1:c.-2567_-2… XM_047430215.1:c.-2567_-2560=	N/A	5 Prime UTR Variant
CCDC28B transcript variant X3	XM_047430217.1:c.-2567_-2… XM_047430217.1:c.-2567_-2560=	N/A	5 Prime UTR Variant
CCDC28B transcript variant X2	XM_011542113.4:c.	N/A	Genic Upstream Transcript Variant
CCDC28B transcript variant X4	XM_017002307.2:c.	N/A	Genic Upstream Transcript Variant
CCDC28B transcript variant X5	XM_017002308.3: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	(G)₈=	delG	dupG	dupGG	dupGGG
GRCh38.p14 chr 1	NC_000001.11:g.32199369_32199376=	NC_000001.11:g.32199376del	NC_000001.11:g.32199376dup	NC_000001.11:g.32199375_32199376dup	NC_000001.11:g.32199374_32199376dup
GRCh37.p13 chr 1	NC_000001.10:g.32664970_32664977=	NC_000001.10:g.32664977del	NC_000001.10:g.32664977dup	NC_000001.10:g.32664976_32664977dup	NC_000001.10:g.32664975_32664977dup
CCDC28B RefSeqGene	NG_012178.1:g.3769_3776=	NG_012178.1:g.3776del	NG_012178.1:g.3776dup	NG_012178.1:g.3775_3776dup	NG_012178.1:g.3774_3776dup
CCDC28B transcript variant X1	XM_047430215.1:c.-2567_-2560=	XM_047430215.1:c.-2560del	XM_047430215.1:c.-2560dup	XM_047430215.1:c.-2561_-2560dup	XM_047430215.1:c.-2562_-2560dup
CCDC28B transcript variant X3	XM_047430217.1:c.-2567_-2560=	XM_047430217.1:c.-2560del	XM_047430217.1:c.-2560dup	XM_047430217.1:c.-2561_-2560dup	XM_047430217.1:c.-2562_-2560dup

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#.

48 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BUSHMAN	ss193095492	Jul 04, 2010 (132)
2	GMI	ss287965473	May 04, 2012 (137)
3	1000GENOMES	ss326020264	May 09, 2011 (134)
4	1000GENOMES	ss326020342	Jan 10, 2018 (151)
5	1000GENOMES	ss326026920	Jan 10, 2018 (151)
6	LUNTER	ss550920727	Apr 25, 2013 (138)
7	LUNTER	ss550922832	Apr 25, 2013 (138)
8	LUNTER	ss552755237	Apr 25, 2013 (138)
9	TISHKOFF	ss553724486	Apr 25, 2013 (138)
10	SSMP	ss663181598	Apr 01, 2015 (144)
11	1000GENOMES	ss1367682662	Aug 21, 2014 (142)
12	EVA_UK10K_ALSPAC	ss1700454077	Apr 01, 2015 (144)
13	EVA_UK10K_TWINSUK	ss1700454180	Apr 01, 2015 (144)
14	EVA_UK10K_TWINSUK	ss1709916940	Apr 01, 2015 (144)
15	EVA_UK10K_ALSPAC	ss1709918909	Apr 01, 2015 (144)
16	HAMMER_LAB	ss1794142133	Sep 08, 2015 (146)
17	SYSTEMSBIOZJU	ss2624327142	Nov 08, 2017 (151)
18	SWEGEN	ss2986568047	Nov 08, 2017 (151)
19	BEROUKHIMLAB	ss3644056225	Oct 11, 2018 (152)
20	EVA_DECODE	ss3686470733	Jul 12, 2019 (153)
21	EVA_DECODE	ss3686470734	Jul 12, 2019 (153)
22	EVA_DECODE	ss3686470735	Jul 12, 2019 (153)
23	ACPOP	ss3726919441	Jul 12, 2019 (153)
24	ACPOP	ss3726919442	Jul 12, 2019 (153)
25	PACBIO	ss3783370402	Jul 12, 2019 (153)
26	PACBIO	ss3789036402	Jul 12, 2019 (153)
27	PACBIO	ss3793909018	Jul 12, 2019 (153)
28	KHV_HUMAN_GENOMES	ss3799032159	Jul 12, 2019 (153)
29	KHV_HUMAN_GENOMES	ss3799032160	Jul 12, 2019 (153)
30	EVA	ss3826100808	Apr 25, 2020 (154)
31	EVA	ss3836438397	Apr 25, 2020 (154)
32	EVA	ss3841843580	Apr 25, 2020 (154)
33	KOGIC	ss3944177787	Apr 25, 2020 (154)
34	KOGIC	ss3944177788	Apr 25, 2020 (154)
35	GNOMAD	ss3990942808	Apr 25, 2021 (155)
36	GNOMAD	ss3990942809	Apr 25, 2021 (155)
37	GNOMAD	ss3990942811	Apr 25, 2021 (155)
38	TOPMED	ss4444275833	Apr 25, 2021 (155)
39	TOMMO_GENOMICS	ss5143228327	Apr 25, 2021 (155)
40	TOMMO_GENOMICS	ss5143228328	Apr 25, 2021 (155)
41	1000G_HIGH_COVERAGE	ss5241731357	Oct 13, 2022 (156)
42	HUGCELL_USP	ss5442855713	Oct 13, 2022 (156)
43	HUGCELL_USP	ss5442855714	Oct 13, 2022 (156)
44	TOMMO_GENOMICS	ss5667769278	Oct 13, 2022 (156)
45	TOMMO_GENOMICS	ss5667769279	Oct 13, 2022 (156)
46	EVA	ss5831755000	Oct 13, 2022 (156)
47	EVA	ss5831755001	Oct 13, 2022 (156)
48	EVA	ss5848846932	Oct 13, 2022 (156)
49	1000Genomes	NC_000001.10 - 32664970	Oct 11, 2018 (152)
50	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 523392 (NC_000001.10:32664969::G 412/3854) Row 523393 (NC_000001.10:32664969:G: 261/3854)	-	Oct 11, 2018 (152)
51	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 523392 (NC_000001.10:32664969::G 412/3854) Row 523393 (NC_000001.10:32664969:G: 261/3854)	-	Oct 11, 2018 (152)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 6871786 (NC_000001.11:32199368::G 11323/139586) Row 6871787 (NC_000001.11:32199368::GG 16/139634) Row 6871789 (NC_000001.11:32199368:G: 17136/139594)	-	Apr 25, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 6871786 (NC_000001.11:32199368::G 11323/139586) Row 6871787 (NC_000001.11:32199368::GG 16/139634) Row 6871789 (NC_000001.11:32199368:G: 17136/139594)	-	Apr 25, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 6871786 (NC_000001.11:32199368::G 11323/139586) Row 6871787 (NC_000001.11:32199368::GG 16/139634) Row 6871789 (NC_000001.11:32199368:G: 17136/139594)	-	Apr 25, 2021 (155)
55	Korean Genome Project Submission ignored due to conflicting rows: Row 555788 (NC_000001.11:32199368:G: 367/1832) Row 555789 (NC_000001.11:32199369::G 10/1832)	-	Apr 25, 2020 (154)
56	Korean Genome Project Submission ignored due to conflicting rows: Row 555788 (NC_000001.11:32199368:G: 367/1832) Row 555789 (NC_000001.11:32199369::G 10/1832)	-	Apr 25, 2020 (154)
57	Northern Sweden Submission ignored due to conflicting rows: Row 204306 (NC_000001.10:32664969::G 81/600) Row 204307 (NC_000001.10:32664969:G: 40/600)	-	Jul 12, 2019 (153)
58	Northern Sweden Submission ignored due to conflicting rows: Row 204306 (NC_000001.10:32664969::G 81/600) Row 204307 (NC_000001.10:32664969:G: 40/600)	-	Jul 12, 2019 (153)
59	8.3KJPN Submission ignored due to conflicting rows: Row 1197634 (NC_000001.10:32664969:G: 3082/16760) Row 1197635 (NC_000001.10:32664969::G 13/16760)	-	Apr 25, 2021 (155)
60	8.3KJPN Submission ignored due to conflicting rows: Row 1197634 (NC_000001.10:32664969:G: 3082/16760) Row 1197635 (NC_000001.10:32664969::G 13/16760)	-	Apr 25, 2021 (155)
61	14KJPN Submission ignored due to conflicting rows: Row 1606382 (NC_000001.11:32199368:G: 5227/28258) Row 1606383 (NC_000001.11:32199368::G 22/28258)	-	Oct 13, 2022 (156)
62	14KJPN Submission ignored due to conflicting rows: Row 1606382 (NC_000001.11:32199368:G: 5227/28258) Row 1606383 (NC_000001.11:32199368::G 22/28258)	-	Oct 13, 2022 (156)
63	TopMed	NC_000001.11 - 32199369	Apr 25, 2021 (155)
64	UK 10K study - Twins Submission ignored due to conflicting rows: Row 523392 (NC_000001.10:32664969::G 436/3708) Row 523393 (NC_000001.10:32664969:G: 248/3708)	-	Oct 11, 2018 (152)
65	UK 10K study - Twins Submission ignored due to conflicting rows: Row 523392 (NC_000001.10:32664969::G 436/3708) Row 523393 (NC_000001.10:32664969:G: 248/3708)	-	Oct 11, 2018 (152)
66	ALFA	NC_000001.11 - 32199369	Apr 25, 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)
rs371998792	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss287965473, ss326020342, ss326026920, ss550922832, ss552755237	NC_000001.9:32437556:G:	NC_000001.11:32199368:GGGGGGGG:GGG… NC_000001.11:32199368:GGGGGGGG:GGGGGGG	(self)
ss663181598, ss1700454077, ss1700454180, ss1794142133, ss2624327142, ss2986568047, ss3644056225, ss3726919442, ss3783370402, ss3789036402, ss3793909018, ss3826100808, ss3836438397, ss5143228327, ss5831755001	NC_000001.10:32664969:G:	NC_000001.11:32199368:GGGGGGGG:GGG… NC_000001.11:32199368:GGGGGGGG:GGGGGGG	(self)
ss553724486	NC_000001.10:32664976:G:	NC_000001.11:32199368:GGGGGGGG:GGG… NC_000001.11:32199368:GGGGGGGG:GGGGGGG	(self)
ss3686470735, ss3799032160, ss3841843580, ss3944177787, ss3990942811, ss5241731357, ss5442855714, ss5667769278, ss5848846932	NC_000001.11:32199368:G:	NC_000001.11:32199368:GGGGGGGG:GGG… NC_000001.11:32199368:GGGGGGGG:GGGGGGG	(self)
10989636578	NC_000001.11:32199368:GGGGGGGG:GGG… NC_000001.11:32199368:GGGGGGGG:GGGGGGG	NC_000001.11:32199368:GGGGGGGG:GGG… NC_000001.11:32199368:GGGGGGGG:GGGGGGG	(self)
ss193095492	NT_032977.10:31613380:G:	NC_000001.11:32199368:GGGGGGGG:GGG… NC_000001.11:32199368:GGGGGGGG:GGGGGGG	(self)
ss326020264, ss550920727	NC_000001.9:32437556::G	NC_000001.11:32199368:GGGGGGGG:GGG… NC_000001.11:32199368:GGGGGGGG:GGGGGGGGG	(self)
976474, ss1367682662, ss3726919441, ss5143228328, ss5831755000	NC_000001.10:32664969::G	NC_000001.11:32199368:GGGGGGGG:GGG… NC_000001.11:32199368:GGGGGGGG:GGGGGGGGG	(self)
ss1709916940, ss1709918909	NC_000001.10:32664970::G	NC_000001.11:32199368:GGGGGGGG:GGG… NC_000001.11:32199368:GGGGGGGG:GGGGGGGGG	(self)
ss3799032159, ss3990942808, ss5442855713, ss5667769279	NC_000001.11:32199368::G	NC_000001.11:32199368:GGGGGGGG:GGG… NC_000001.11:32199368:GGGGGGGG:GGGGGGGGG	(self)
10989636578	NC_000001.11:32199368:GGGGGGGG:GGG… NC_000001.11:32199368:GGGGGGGG:GGGGGGGGG	NC_000001.11:32199368:GGGGGGGG:GGG… NC_000001.11:32199368:GGGGGGGG:GGGGGGGGG	(self)
ss3686470734, ss3944177788	NC_000001.11:32199369::G	NC_000001.11:32199368:GGGGGGGG:GGG… NC_000001.11:32199368:GGGGGGGG:GGGGGGGGG	(self)
ss3990942809	NC_000001.11:32199368::GG	NC_000001.11:32199368:GGGGGGGG:GGG… NC_000001.11:32199368:GGGGGGGG:GGGGGGGGGG	(self)
10989636578	NC_000001.11:32199368:GGGGGGGG:GGG… NC_000001.11:32199368:GGGGGGGG:GGGGGGGGGG	NC_000001.11:32199368:GGGGGGGG:GGG… NC_000001.11:32199368:GGGGGGGG:GGGGGGGGGG	(self)
ss3686470733	NC_000001.11:32199369::GG	NC_000001.11:32199368:GGGGGGGG:GGG… NC_000001.11:32199368:GGGGGGGG:GGGGGGGGGG	(self)
7882168, ss4444275833	NC_000001.11:32199368::GGG	NC_000001.11:32199368:GGGGGGGG:GGG… NC_000001.11:32199368:GGGGGGGG:GGGGGGGGGGG	(self)
10989636578	NC_000001.11:32199368:GGGGGGGG:GGG… NC_000001.11:32199368:GGGGGGGG:GGGGGGGGGGG	NC_000001.11:32199368:GGGGGGGG:GGG… NC_000001.11:32199368:GGGGGGGG:GGGGGGGGGGG	(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 rs113383928

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs113383928