Name: rs9302237
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.

rs9302237

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr15:65186539-65186556 (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)₆ / del(A)₄ / delAAA / delAA…
del(A)₆ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA
Variation Type: Indel Insertion and Deletion
Frequency: (A)₁₈=0.1715 (859/5008, 1000G)
(A)₁₈=0.0003 (1/3854, ALSPAC)
(A)₁₈=0.0000 (0/3708, TWINSUK) (+ 6 more)
del(A)₆=0.0 (0/4, ALFA)
delAAA=0.0 (0/4, ALFA)
delAA=0.0 (0/4, ALFA)
delA=0.0 (0/4, ALFA)
dupA=0.0 (0/4, ALFA)
dupAA=0.0 (0/4, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CLPX : 2KB Upstream 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	4	AAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
European	Sub	0	AAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
African	Sub	4	AAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
African Others	Sub	0	AAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
African American	Sub	4	AAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Asian	Sub	0	AAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
East Asian	Sub	0	AAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	0	AAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 2	Sub	0	AAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
South Asian	Sub	0	AAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other	Sub	0	AAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=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
1000Genomes	Global	Study-wide	5008	(A)₁₈=0.1715	delA=0.8285
1000Genomes	African	Sub	1322	(A)₁₈=0.2557	delA=0.7443
1000Genomes	East Asian	Sub	1008	(A)₁₈=0.0317	delA=0.9683
1000Genomes	Europe	Sub	1006	(A)₁₈=0.2217	delA=0.7783
1000Genomes	South Asian	Sub	978	(A)₁₈=0.132	delA=0.868
1000Genomes	American	Sub	694	(A)₁₈=0.197	delA=0.803
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(A)₁₈=0.0003	delAA=0.9997
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	(A)₁₈=0.0000	delAA=1.0000
Allele Frequency Aggregator	Total	Global	4	(A)₁₈=1.0	del(A)₆=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0
Allele Frequency Aggregator	African	Sub	4	(A)₁₈=1.0	del(A)₆=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0
Allele Frequency Aggregator	European	Sub	0	(A)₁₈=0	del(A)₆=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0
Allele Frequency Aggregator	Latin American 1	Sub	0	(A)₁₈=0	del(A)₆=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0
Allele Frequency Aggregator	Latin American 2	Sub	0	(A)₁₈=0	del(A)₆=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0
Allele Frequency Aggregator	South Asian	Sub	0	(A)₁₈=0	del(A)₆=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0
Allele Frequency Aggregator	Other	Sub	0	(A)₁₈=0	del(A)₆=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0
Allele Frequency Aggregator	Asian	Sub	0	(A)₁₈=0	del(A)₆=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0

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 15	NC_000015.10:g.65186551_65186556del
GRCh38.p14 chr 15	NC_000015.10:g.65186553_65186556del
GRCh38.p14 chr 15	NC_000015.10:g.65186554_65186556del
GRCh38.p14 chr 15	NC_000015.10:g.65186555_65186556del
GRCh38.p14 chr 15	NC_000015.10:g.65186556del
GRCh38.p14 chr 15	NC_000015.10:g.65186556dup
GRCh38.p14 chr 15	NC_000015.10:g.65186555_65186556dup
GRCh37.p13 chr 15	NC_000015.9:g.65478889_65478894del
GRCh37.p13 chr 15	NC_000015.9:g.65478891_65478894del
GRCh37.p13 chr 15	NC_000015.9:g.65478892_65478894del
GRCh37.p13 chr 15	NC_000015.9:g.65478893_65478894del
GRCh37.p13 chr 15	NC_000015.9:g.65478894del
GRCh37.p13 chr 15	NC_000015.9:g.65478894dup
GRCh37.p13 chr 15	NC_000015.9:g.65478893_65478894dup

Gene: CLPX, caseinolytic mitochondrial matrix peptidase chaperone subunit X (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
CLPX transcript variant 1	NM_006660.5:c.	N/A	Upstream Transcript Variant
CLPX transcript variant 2	NR_133680.2:n.	N/A	Upstream Transcript Variant
CLPX transcript variant X1	XM_011521164.4:c.	N/A	Upstream Transcript Variant
CLPX transcript variant X2	XR_931743.4:n.	N/A	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	(A)₁₈=	del(A)₆	del(A)₄	delAAA	delAA	delA	dupA	dupAA
GRCh38.p14 chr 15	NC_000015.10:g.65186539_65186556=	NC_000015.10:g.65186551_65186556del	NC_000015.10:g.65186553_65186556del	NC_000015.10:g.65186554_65186556del	NC_000015.10:g.65186555_65186556del	NC_000015.10:g.65186556del	NC_000015.10:g.65186556dup	NC_000015.10:g.65186555_65186556dup
GRCh37.p13 chr 15	NC_000015.9:g.65478877_65478894=	NC_000015.9:g.65478889_65478894del	NC_000015.9:g.65478891_65478894del	NC_000015.9:g.65478892_65478894del	NC_000015.9:g.65478893_65478894del	NC_000015.9:g.65478894del	NC_000015.9:g.65478894dup	NC_000015.9:g.65478893_65478894dup

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#.

54 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80796297	Dec 15, 2007 (130)
2	HGSV	ss81504483	Dec 15, 2007 (130)
3	HGSV	ss82144881	Dec 15, 2007 (130)
4	HGSV	ss83897359	Dec 15, 2007 (130)
5	HUMANGENOME_JCVI	ss95661503	Mar 15, 2016 (147)
6	BUSHMAN	ss193388159	Mar 15, 2016 (147)
7	GMI	ss287929649	May 09, 2011 (136)
8	GMI	ss289263259	May 04, 2012 (137)
9	SSMP	ss664281861	Apr 01, 2015 (144)
10	BILGI_BIOE	ss666652221	Apr 25, 2013 (138)
11	1000GENOMES	ss1375006961	Aug 21, 2014 (142)
12	DDI	ss1536809817	Apr 01, 2015 (144)
13	EVA_UK10K_ALSPAC	ss1708332386	Apr 01, 2015 (144)
14	EVA_UK10K_TWINSUK	ss1708332472	Apr 01, 2015 (144)
15	SWEGEN	ss3013445006	Nov 08, 2017 (151)
16	MCHAISSO	ss3064660454	Nov 08, 2017 (151)
17	BEROUKHIMLAB	ss3644389608	Oct 12, 2018 (152)
18	BIOINF_KMB_FNS_UNIBA	ss3645388344	Oct 12, 2018 (152)
19	URBANLAB	ss3650377425	Oct 12, 2018 (152)
20	EVA_DECODE	ss3698090547	Jul 13, 2019 (153)
21	EVA_DECODE	ss3698090548	Jul 13, 2019 (153)
22	EVA_DECODE	ss3698090549	Jul 13, 2019 (153)
23	ACPOP	ss3741010975	Jul 13, 2019 (153)
24	ACPOP	ss3741010976	Jul 13, 2019 (153)
25	PACBIO	ss3787876254	Jul 13, 2019 (153)
26	PACBIO	ss3787876255	Jul 13, 2019 (153)
27	PACBIO	ss3792883905	Jul 13, 2019 (153)
28	PACBIO	ss3797768471	Jul 13, 2019 (153)
29	KHV_HUMAN_GENOMES	ss3818525431	Jul 13, 2019 (153)
30	EVA	ss3834286042	Apr 27, 2020 (154)
31	GNOMAD	ss4290533055	Apr 27, 2021 (155)
32	GNOMAD	ss4290533056	Apr 27, 2021 (155)
33	GNOMAD	ss4290533057	Apr 27, 2021 (155)
34	GNOMAD	ss4290533058	Apr 27, 2021 (155)
35	GNOMAD	ss4290533059	Apr 27, 2021 (155)
36	GNOMAD	ss4290533060	Apr 27, 2021 (155)
37	GNOMAD	ss4290533061	Apr 27, 2021 (155)
38	TOMMO_GENOMICS	ss5216657350	Apr 27, 2021 (155)
39	TOMMO_GENOMICS	ss5216657351	Apr 27, 2021 (155)
40	TOMMO_GENOMICS	ss5216657352	Apr 27, 2021 (155)
41	TOMMO_GENOMICS	ss5216657353	Apr 27, 2021 (155)
42	1000G_HIGH_COVERAGE	ss5298793249	Oct 16, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5298793250	Oct 16, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5298793251	Oct 16, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5298793252	Oct 16, 2022 (156)
46	HUGCELL_USP	ss5492488158	Oct 16, 2022 (156)
47	HUGCELL_USP	ss5492488159	Oct 16, 2022 (156)
48	TOMMO_GENOMICS	ss5770599768	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5770599769	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5770599770	Oct 16, 2022 (156)
51	TOMMO_GENOMICS	ss5770599771	Oct 16, 2022 (156)
52	EVA	ss5828338869	Oct 16, 2022 (156)
53	EVA	ss5876284149	Oct 16, 2022 (156)
54	EVA	ss5980876074	Oct 16, 2022 (156)
55	1000Genomes	NC_000015.9 - 65478877	Oct 12, 2018 (152)
56	The Avon Longitudinal Study of Parents and Children	NC_000015.9 - 65478877	Oct 12, 2018 (152)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 472013305 (NC_000015.10:65186538::A 63/130282) Row 472013306 (NC_000015.10:65186538::AA 15/130282) Row 472013307 (NC_000015.10:65186538:A: 27567/129020)...	-	Apr 27, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 472013305 (NC_000015.10:65186538::A 63/130282) Row 472013306 (NC_000015.10:65186538::AA 15/130282) Row 472013307 (NC_000015.10:65186538:A: 27567/129020)...	-	Apr 27, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 472013305 (NC_000015.10:65186538::A 63/130282) Row 472013306 (NC_000015.10:65186538::AA 15/130282) Row 472013307 (NC_000015.10:65186538:A: 27567/129020)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 472013305 (NC_000015.10:65186538::A 63/130282) Row 472013306 (NC_000015.10:65186538::AA 15/130282) Row 472013307 (NC_000015.10:65186538:A: 27567/129020)...	-	Apr 27, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 472013305 (NC_000015.10:65186538::A 63/130282) Row 472013306 (NC_000015.10:65186538::AA 15/130282) Row 472013307 (NC_000015.10:65186538:A: 27567/129020)...	-	Apr 27, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 472013305 (NC_000015.10:65186538::A 63/130282) Row 472013306 (NC_000015.10:65186538::AA 15/130282) Row 472013307 (NC_000015.10:65186538:A: 27567/129020)...	-	Apr 27, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 472013305 (NC_000015.10:65186538::A 63/130282) Row 472013306 (NC_000015.10:65186538::AA 15/130282) Row 472013307 (NC_000015.10:65186538:A: 27567/129020)...	-	Apr 27, 2021 (155)
64	Northern Sweden Submission ignored due to conflicting rows: Row 14295840 (NC_000015.9:65478876:AA: 474/580) Row 14295841 (NC_000015.9:65478876:A: 28/580)	-	Jul 13, 2019 (153)
65	Northern Sweden Submission ignored due to conflicting rows: Row 14295840 (NC_000015.9:65478876:AA: 474/580) Row 14295841 (NC_000015.9:65478876:A: 28/580)	-	Jul 13, 2019 (153)
66	8.3KJPN Submission ignored due to conflicting rows: Row 74626657 (NC_000015.9:65478876:AA: 16577/16760) Row 74626658 (NC_000015.9:65478876:A: 152/16760) Row 74626659 (NC_000015.9:65478876:AAA: 5/16760)...	-	Apr 27, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 74626657 (NC_000015.9:65478876:AA: 16577/16760) Row 74626658 (NC_000015.9:65478876:A: 152/16760) Row 74626659 (NC_000015.9:65478876:AAA: 5/16760)...	-	Apr 27, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 74626657 (NC_000015.9:65478876:AA: 16577/16760) Row 74626658 (NC_000015.9:65478876:A: 152/16760) Row 74626659 (NC_000015.9:65478876:AAA: 5/16760)...	-	Apr 27, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 74626657 (NC_000015.9:65478876:AA: 16577/16760) Row 74626658 (NC_000015.9:65478876:A: 152/16760) Row 74626659 (NC_000015.9:65478876:AAA: 5/16760)...	-	Apr 27, 2021 (155)
70	14KJPN Submission ignored due to conflicting rows: Row 104436872 (NC_000015.10:65186538:AA: 27957/28256) Row 104436873 (NC_000015.10:65186538:A: 257/28256) Row 104436874 (NC_000015.10:65186538:AAA: 11/28256)...	-	Oct 16, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 104436872 (NC_000015.10:65186538:AA: 27957/28256) Row 104436873 (NC_000015.10:65186538:A: 257/28256) Row 104436874 (NC_000015.10:65186538:AAA: 11/28256)...	-	Oct 16, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 104436872 (NC_000015.10:65186538:AA: 27957/28256) Row 104436873 (NC_000015.10:65186538:A: 257/28256) Row 104436874 (NC_000015.10:65186538:AAA: 11/28256)...	-	Oct 16, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 104436872 (NC_000015.10:65186538:AA: 27957/28256) Row 104436873 (NC_000015.10:65186538:A: 257/28256) Row 104436874 (NC_000015.10:65186538:AAA: 11/28256)...	-	Oct 16, 2022 (156)
74	UK 10K study - Twins	NC_000015.9 - 65478877	Oct 12, 2018 (152)
75	ALFA	NC_000015.10 - 65186539	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).

Associated ID	History Updated (Build)
rs59882551	May 25, 2008 (130)
rs147818437	Oct 19, 2011 (136)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5216657353	NC_000015.9:65478876:AAAAAA:	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4290533061, ss5770599771	NC_000015.10:65186538:AAAAAA:	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
12969278805	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4290533060	NC_000015.10:65186538:AAAA:	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3787876254, ss5216657352	NC_000015.9:65478876:AAA:	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3698090549, ss4290533059, ss5298793252, ss5770599770	NC_000015.10:65186538:AAA:	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
12969278805	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss95661503	NT_010194.17:36269445:AAA:	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss289263259	NC_000015.8:63265929:AA:	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss80796297, ss81504483, ss82144881, ss83897359	NC_000015.8:63265945:AA:	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
37175092, 37175092, ss664281861, ss666652221, ss1536809817, ss1708332386, ss1708332472, ss3013445006, ss3644389608, ss3741010975, ss3787876255, ss3792883905, ss3797768471, ss5216657350, ss5828338869, ss5980876074	NC_000015.9:65478876:AA:	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3064660454, ss3645388344, ss3650377425, ss4290533058, ss5298793249, ss5492488158, ss5770599768, ss5876284149	NC_000015.10:65186538:AA:	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
12969278805	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3698090548	NC_000015.10:65186539:AA:	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss193388159	NT_010194.17:36269433:AA:	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
66953412, ss1375006961, ss3741010976, ss3834286042, ss5216657351	NC_000015.9:65478876:A:	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3818525431, ss4290533057, ss5298793250, ss5492488159, ss5770599769	NC_000015.10:65186538:A:	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
12969278805	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3698090547	NC_000015.10:65186540:A:	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss287929649	NT_010194.17:36269433:A:	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss95661503	NT_010194.17:36269445:AAA:AA	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4290533055, ss5298793251	NC_000015.10:65186538::A	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
12969278805	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4290533056	NC_000015.10:65186538::AA	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
12969278805	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000015.10:65186538:AAAAAAAAAAAA… NC_000015.10:65186538:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(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 rs9302237

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

rs9302237