Name: rs10933436
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.

rs10933436

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:233133771 (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: C>A / C>G / C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.481306 (127397/264690, TOPMED)
A=0.465566 (79122/169948, ALFA)
A=0.470701 (65787/139764, GnomAD) (+ 20 more)
A=0.48357 (38038/78660, PAGE_STUDY)
A=0.45378 (12822/28256, 14KJPN)
A=0.45937 (7699/16760, 8.3KJPN)
A=0.4878 (3124/6404, 1000G_30x)
A=0.4792 (2400/5008, 1000G)
A=0.4020 (1801/4480, Estonian)
A=0.4455 (1717/3854, ALSPAC)
A=0.4474 (1659/3708, TWINSUK)
A=0.4764 (1395/2928, KOREAN)
A=0.4727 (866/1832, Korea1K)
A=0.433 (432/998, GoNL)
A=0.481 (380/790, PRJEB37584)
A=0.473 (284/600, NorthernSweden)
C=0.340 (130/382, SGDP_PRJ)
C=0.435 (140/322, HapMap)
C=0.435 (94/216, Qatari)
C=0.439 (94/214, Vietnamese)
C=0.35 (18/52, Ancient Sardinia)
A=0.30 (12/40, GENOME_DK)
C=0.39 (15/38, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: INPP5D : 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: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	170042	C=0.534350	A=0.465650, G=0.000000
European	Sub	152614	C=0.536268	A=0.463732, G=0.000000
African	Sub	3930	C=0.4850	A=0.5150, G=0.0000
African Others	Sub	148	C=0.473	A=0.527, G=0.000
African American	Sub	3782	C=0.4855	A=0.5145, G=0.0000
Asian	Sub	3290	C=0.5304	A=0.4696, G=0.0000
East Asian	Sub	2640	C=0.5417	A=0.4583, G=0.0000
Other Asian	Sub	650	C=0.485	A=0.515, G=0.000
Latin American 1	Sub	442	C=0.538	A=0.462, G=0.000
Latin American 2	Sub	950	C=0.647	A=0.353, G=0.000
South Asian	Sub	280	C=0.471	A=0.529, G=0.000
Other	Sub	8536	C=0.5136	A=0.4864, G=0.0000

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	C=0.518694	A=0.481306
Allele Frequency Aggregator	Total	Global	169948	C=0.534434	A=0.465566, G=0.000000
Allele Frequency Aggregator	European	Sub	152538	C=0.536345	A=0.463655, G=0.000000
Allele Frequency Aggregator	Other	Sub	8518	C=0.5139	A=0.4861, G=0.0000
Allele Frequency Aggregator	African	Sub	3930	C=0.4850	A=0.5150, G=0.0000
Allele Frequency Aggregator	Asian	Sub	3290	C=0.5304	A=0.4696, G=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	950	C=0.647	A=0.353, G=0.000
Allele Frequency Aggregator	Latin American 1	Sub	442	C=0.538	A=0.462, G=0.000
Allele Frequency Aggregator	South Asian	Sub	280	C=0.471	A=0.529, G=0.000
gnomAD - Genomes	Global	Study-wide	139764	C=0.529299	A=0.470701
gnomAD - Genomes	European	Sub	75722	C=0.56375	A=0.43625
gnomAD - Genomes	African	Sub	41848	C=0.45866	A=0.54134
gnomAD - Genomes	American	Sub	13616	C=0.59812	A=0.40188
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	C=0.4205	A=0.5795
gnomAD - Genomes	East Asian	Sub	3110	C=0.4740	A=0.5260
gnomAD - Genomes	Other	Sub	2146	C=0.5033	A=0.4967
The PAGE Study	Global	Study-wide	78660	C=0.51643	A=0.48357
The PAGE Study	AfricanAmerican	Sub	32506	C=0.46431	A=0.53569
The PAGE Study	Mexican	Sub	10802	C=0.65145	A=0.34855
The PAGE Study	Asian	Sub	8312	C=0.5301	A=0.4699
The PAGE Study	PuertoRican	Sub	7912	C=0.4862	A=0.5138
The PAGE Study	NativeHawaiian	Sub	4532	C=0.5313	A=0.4687
The PAGE Study	Cuban	Sub	4222	C=0.4950	A=0.5050
The PAGE Study	Dominican	Sub	3828	C=0.4909	A=0.5091
The PAGE Study	CentralAmerican	Sub	2448	C=0.6103	A=0.3897
The PAGE Study	SouthAmerican	Sub	1982	C=0.6070	A=0.3930
The PAGE Study	NativeAmerican	Sub	1260	C=0.5794	A=0.4206
The PAGE Study	SouthAsian	Sub	856	C=0.508	A=0.492
14KJPN	JAPANESE	Study-wide	28256	C=0.54622	A=0.45378
8.3KJPN	JAPANESE	Study-wide	16760	C=0.54063	A=0.45937
1000Genomes_30x	Global	Study-wide	6404	C=0.5122	A=0.4878
1000Genomes_30x	African	Sub	1786	C=0.4496	A=0.5504
1000Genomes_30x	Europe	Sub	1266	C=0.5253	A=0.4747
1000Genomes_30x	South Asian	Sub	1202	C=0.5233	A=0.4767
1000Genomes_30x	East Asian	Sub	1170	C=0.4949	A=0.5051
1000Genomes_30x	American	Sub	980	C=0.616	A=0.384
1000Genomes	Global	Study-wide	5008	C=0.5208	A=0.4792
1000Genomes	African	Sub	1322	C=0.4614	A=0.5386
1000Genomes	East Asian	Sub	1008	C=0.5030	A=0.4970
1000Genomes	Europe	Sub	1006	C=0.5427	A=0.4573
1000Genomes	South Asian	Sub	978	C=0.530	A=0.470
1000Genomes	American	Sub	694	C=0.615	A=0.385
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.5980	A=0.4020
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.5545	A=0.4455
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.5526	A=0.4474
KOREAN population from KRGDB	KOREAN	Study-wide	2928	C=0.5236	A=0.4764, T=0.0000
Korean Genome Project	KOREAN	Study-wide	1832	C=0.5273	A=0.4727
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.567	A=0.433
CNV burdens in cranial meningiomas	Global	Study-wide	790	C=0.519	A=0.481
CNV burdens in cranial meningiomas	CRM	Sub	790	C=0.519	A=0.481
Northern Sweden	ACPOP	Study-wide	600	C=0.527	A=0.473
SGDP_PRJ	Global	Study-wide	382	C=0.340	A=0.660
HapMap	Global	Study-wide	322	C=0.435	A=0.565
HapMap	African	Sub	118	C=0.398	A=0.602
HapMap	American	Sub	116	C=0.405	A=0.595
HapMap	Asian	Sub	88	C=0.52	A=0.48
Qatari	Global	Study-wide	216	C=0.435	A=0.565
A Vietnamese Genetic Variation Database	Global	Study-wide	214	C=0.439	A=0.561
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	52	C=0.35	A=0.65
The Danish reference pan genome	Danish	Study-wide	40	C=0.70	A=0.30
Siberian	Global	Study-wide	38	C=0.39	A=0.61

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 2	NC_000002.12:g.233133771C>A
GRCh38.p14 chr 2	NC_000002.12:g.233133771C>G
GRCh38.p14 chr 2	NC_000002.12:g.233133771C>T
GRCh37.p13 chr 2	NC_000002.11:g.233998481C>A
GRCh37.p13 chr 2	NC_000002.11:g.233998481C>G
GRCh37.p13 chr 2	NC_000002.11:g.233998481C>T
INPP5D RefSeqGene	NG_033988.1:g.78805C>A
INPP5D RefSeqGene	NG_033988.1:g.78805C>G
INPP5D RefSeqGene	NG_033988.1:g.78805C>T
GRCh38.p14 chr 2 fix patch HG2232_PATCH	NW_011332690.1:g.79109C>A
GRCh38.p14 chr 2 fix patch HG2232_PATCH	NW_011332690.1:g.79109C>G
GRCh38.p14 chr 2 fix patch HG2232_PATCH	NW_011332690.1:g.79109C>T

Gene: INPP5D, inositol polyphosphate-5-phosphatase D (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
INPP5D transcript variant 1	NM_001017915.3:c.665+3123… NM_001017915.3:c.665+3123C>A	N/A	Intron Variant
INPP5D transcript variant 2	NM_005541.5:c.662+3123C>A	N/A	Intron Variant
INPP5D transcript variant X1	XM_047444219.1:c.665+3123… XM_047444219.1:c.665+3123C>A	N/A	Intron Variant
INPP5D transcript variant X2	XM_047444220.1:c.662+3123… XM_047444220.1:c.662+3123C>A	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	C=	A	G	T
GRCh38.p14 chr 2	NC_000002.12:g.233133771=	NC_000002.12:g.233133771C>A	NC_000002.12:g.233133771C>G	NC_000002.12:g.233133771C>T
GRCh37.p13 chr 2	NC_000002.11:g.233998481=	NC_000002.11:g.233998481C>A	NC_000002.11:g.233998481C>G	NC_000002.11:g.233998481C>T
INPP5D RefSeqGene	NG_033988.1:g.78805=	NG_033988.1:g.78805C>A	NG_033988.1:g.78805C>G	NG_033988.1:g.78805C>T
GRCh38.p14 chr 2 fix patch HG2232_PATCH	NW_011332690.1:g.79109=	NW_011332690.1:g.79109C>A	NW_011332690.1:g.79109C>G	NW_011332690.1:g.79109C>T
INPP5D transcript variant 1	NM_001017915.3:c.665+3123=	NM_001017915.3:c.665+3123C>A	NM_001017915.3:c.665+3123C>G	NM_001017915.3:c.665+3123C>T
INPP5D transcript variant 2	NM_005541.5:c.662+3123=	NM_005541.5:c.662+3123C>A	NM_005541.5:c.662+3123C>G	NM_005541.5:c.662+3123C>T
INPP5D transcript variant X1	XM_047444219.1:c.665+3123=	XM_047444219.1:c.665+3123C>A	XM_047444219.1:c.665+3123C>G	XM_047444219.1:c.665+3123C>T
INPP5D transcript variant X2	XM_047444220.1:c.662+3123=	XM_047444220.1:c.662+3123C>A	XM_047444220.1:c.662+3123C>G	XM_047444220.1:c.662+3123C>T

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#.

103 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	CSHL-HAPMAP	ss16834325	Feb 27, 2004 (120)
2	CSHL-HAPMAP	ss17647740	Feb 27, 2004 (120)
3	SSAHASNP	ss21691686	Apr 05, 2004 (121)
4	ABI	ss44282684	Mar 13, 2006 (126)
5	ILLUMINA	ss65816914	Oct 16, 2006 (127)
6	BCMHGSC_JDW	ss91588819	Mar 24, 2008 (129)
7	BGI	ss103698241	Dec 01, 2009 (131)
8	1000GENOMES	ss110958800	Jan 25, 2009 (130)
9	1000GENOMES	ss111819358	Jan 25, 2009 (130)
10	ENSEMBL	ss138650940	Dec 01, 2009 (131)
11	GMI	ss154863779	Dec 01, 2009 (131)
12	ENSEMBL	ss161244669	Dec 01, 2009 (131)
13	COMPLETE_GENOMICS	ss165692410	Jul 04, 2010 (132)
14	COMPLETE_GENOMICS	ss165962201	Jul 04, 2010 (132)
15	COMPLETE_GENOMICS	ss167603601	Jul 04, 2010 (132)
16	BUSHMAN	ss201890010	Jul 04, 2010 (132)
17	1000GENOMES	ss219878728	Jul 14, 2010 (132)
18	1000GENOMES	ss231633976	Jul 14, 2010 (132)
19	1000GENOMES	ss239081783	Jul 15, 2010 (132)
20	BL	ss253933765	May 09, 2011 (134)
21	GMI	ss276942777	May 04, 2012 (137)
22	GMI	ss284562408	Apr 25, 2013 (138)
23	PJP	ss292510108	May 09, 2011 (134)
24	ILLUMINA	ss410890287	Sep 17, 2011 (135)
25	EXOME_CHIP	ss491333156	May 04, 2012 (137)
26	TISHKOFF	ss556302181	Apr 25, 2013 (138)
27	SSMP	ss649963028	Apr 25, 2013 (138)
28	ILLUMINA	ss780680819	Sep 08, 2015 (146)
29	ILLUMINA	ss783354110	Sep 08, 2015 (146)
30	EVA-GONL	ss978083863	Aug 21, 2014 (142)
31	JMKIDD_LAB	ss1070032629	Aug 21, 2014 (142)
32	1000GENOMES	ss1302115454	Aug 21, 2014 (142)
33	DDI	ss1428948657	Apr 01, 2015 (144)
34	EVA_GENOME_DK	ss1579371804	Apr 01, 2015 (144)
35	EVA_DECODE	ss1587544061	Apr 01, 2015 (144)
36	EVA_UK10K_ALSPAC	ss1606047682	Apr 01, 2015 (144)
37	EVA_UK10K_TWINSUK	ss1649041715	Apr 01, 2015 (144)
38	ILLUMINA	ss1752344764	Sep 08, 2015 (146)
39	HAMMER_LAB	ss1798560652	Sep 08, 2015 (146)
40	ILLUMINA	ss1917761390	Feb 12, 2016 (147)
41	WEILL_CORNELL_DGM	ss1921331396	Feb 12, 2016 (147)
42	ILLUMINA	ss1946069753	Feb 12, 2016 (147)
43	ILLUMINA	ss1958517925	Feb 12, 2016 (147)
44	GENOMED	ss1969054731	Jul 19, 2016 (147)
45	JJLAB	ss2021213984	Sep 14, 2016 (149)
46	USC_VALOUEV	ss2149279980	Dec 20, 2016 (150)
47	HUMAN_LONGEVITY	ss2240125974	Dec 20, 2016 (150)
48	SYSTEMSBIOZJU	ss2625107040	Nov 08, 2017 (151)
49	ILLUMINA	ss2633754724	Nov 08, 2017 (151)
50	GRF	ss2703932192	Nov 08, 2017 (151)
51	GNOMAD	ss2787659739	Nov 08, 2017 (151)
52	AFFY	ss2985203630	Nov 08, 2017 (151)
53	AFFY	ss2985825020	Nov 08, 2017 (151)
54	SWEGEN	ss2991551090	Nov 08, 2017 (151)
55	ILLUMINA	ss3022082471	Nov 08, 2017 (151)
56	BIOINF_KMB_FNS_UNIBA	ss3024367149	Nov 08, 2017 (151)
57	CSHL	ss3344796315	Nov 08, 2017 (151)
58	ILLUMINA	ss3628312977	Oct 11, 2018 (152)
59	ILLUMINA	ss3634817782	Oct 11, 2018 (152)
60	ILLUMINA	ss3640525081	Oct 11, 2018 (152)
61	ILLUMINA	ss3644772460	Oct 11, 2018 (152)
62	ILLUMINA	ss3652534604	Oct 11, 2018 (152)
63	ILLUMINA	ss3653971634	Oct 11, 2018 (152)
64	EGCUT_WGS	ss3659449227	Jul 13, 2019 (153)
65	EVA_DECODE	ss3706257297	Jul 13, 2019 (153)
66	ILLUMINA	ss3725884247	Jul 13, 2019 (153)
67	ACPOP	ss3729477032	Jul 13, 2019 (153)
68	ILLUMINA	ss3744488732	Jul 13, 2019 (153)
69	ILLUMINA	ss3745117674	Jul 13, 2019 (153)
70	EVA	ss3758228706	Jul 13, 2019 (153)
71	PAGE_CC	ss3770995883	Jul 13, 2019 (153)
72	ILLUMINA	ss3772614053	Jul 13, 2019 (153)
73	PACBIO	ss3784186852	Jul 13, 2019 (153)
74	PACBIO	ss3789720410	Jul 13, 2019 (153)
75	PACBIO	ss3794593860	Jul 13, 2019 (153)
76	KHV_HUMAN_GENOMES	ss3802591471	Jul 13, 2019 (153)
77	EVA	ss3827567475	Apr 25, 2020 (154)
78	EVA	ss3837204094	Apr 25, 2020 (154)
79	EVA	ss3842626739	Apr 25, 2020 (154)
80	SGDP_PRJ	ss3854844414	Apr 25, 2020 (154)
81	KRGDB	ss3900591996	Apr 25, 2020 (154)
82	KOGIC	ss3950325475	Apr 25, 2020 (154)
83	EVA	ss3984499814	Apr 26, 2021 (155)
84	EVA	ss3984961225	Apr 26, 2021 (155)
85	TOPMED	ss4548677406	Apr 26, 2021 (155)
86	TOMMO_GENOMICS	ss5157034660	Apr 26, 2021 (155)
87	1000G_HIGH_COVERAGE	ss5252446728	Oct 12, 2022 (156)
88	EVA	ss5314817146	Oct 12, 2022 (156)
89	EVA	ss5336794075	Oct 12, 2022 (156)
90	HUGCELL_USP	ss5452016995	Oct 12, 2022 (156)
91	EVA	ss5506835932	Oct 12, 2022 (156)
92	1000G_HIGH_COVERAGE	ss5529994853	Oct 12, 2022 (156)
93	SANFORD_IMAGENETICS	ss5624475318	Oct 12, 2022 (156)
94	SANFORD_IMAGENETICS	ss5631189387	Oct 12, 2022 (156)
95	TOMMO_GENOMICS	ss5688079770	Oct 12, 2022 (156)
96	YY_MCH	ss5803323702	Oct 12, 2022 (156)
97	EVA	ss5821754112	Oct 12, 2022 (156)
98	EVA	ss5847207645	Oct 12, 2022 (156)
99	EVA	ss5847907574	Oct 12, 2022 (156)
100	EVA	ss5852999477	Oct 12, 2022 (156)
101	EVA	ss5935181818	Oct 12, 2022 (156)
102	EVA	ss5957454146	Oct 12, 2022 (156)
103	EVA	ss5979603980	Oct 12, 2022 (156)
104	1000Genomes	NC_000002.11 - 233998481	Oct 11, 2018 (152)
105	1000Genomes_30x	NC_000002.12 - 233133771	Oct 12, 2022 (156)
106	The Avon Longitudinal Study of Parents and Children	NC_000002.11 - 233998481	Oct 11, 2018 (152)
107	Genetic variation in the Estonian population	NC_000002.11 - 233998481	Oct 11, 2018 (152)
108	The Danish reference pan genome	NC_000002.11 - 233998481	Apr 25, 2020 (154)
109	gnomAD - Genomes	NC_000002.12 - 233133771	Apr 26, 2021 (155)
110	Genome of the Netherlands Release 5	NC_000002.11 - 233998481	Apr 25, 2020 (154)
111	HapMap	NC_000002.12 - 233133771	Apr 25, 2020 (154)
112	KOREAN population from KRGDB	NC_000002.11 - 233998481	Apr 25, 2020 (154)
113	Korean Genome Project	NC_000002.12 - 233133771	Apr 25, 2020 (154)
114	Northern Sweden	NC_000002.11 - 233998481	Jul 13, 2019 (153)
115	The PAGE Study	NC_000002.12 - 233133771	Jul 13, 2019 (153)
116	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000002.11 - 233998481	Apr 26, 2021 (155)
117	CNV burdens in cranial meningiomas	NC_000002.11 - 233998481	Apr 26, 2021 (155)
118	Qatari	NC_000002.11 - 233998481	Apr 25, 2020 (154)
119	SGDP_PRJ	NC_000002.11 - 233998481	Apr 25, 2020 (154)
120	Siberian	NC_000002.11 - 233998481	Apr 25, 2020 (154)
121	8.3KJPN	NC_000002.11 - 233998481	Apr 26, 2021 (155)
122	14KJPN	NC_000002.12 - 233133771	Oct 12, 2022 (156)
123	TopMed	NC_000002.12 - 233133771	Apr 26, 2021 (155)
124	UK 10K study - Twins	NC_000002.11 - 233998481	Oct 11, 2018 (152)
125	A Vietnamese Genetic Variation Database	NC_000002.11 - 233998481	Jul 13, 2019 (153)
126	ALFA	NC_000002.12 - 233133771	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss91588819, ss110958800, ss111819358, ss165692410, ss165962201, ss167603601, ss201890010, ss253933765, ss276942777, ss284562408, ss292510108, ss1587544061	NC_000002.10:233706724:C:A	NC_000002.12:233133770:C:A	(self)
13237959, 7331980, 5187475, 5536743, 3212482, 7769390, 2761897, 187152, 49152, 3373326, 6861394, 1796334, 15003967, 7331980, 1591587, ss219878728, ss231633976, ss239081783, ss491333156, ss556302181, ss649963028, ss780680819, ss783354110, ss978083863, ss1070032629, ss1302115454, ss1428948657, ss1579371804, ss1606047682, ss1649041715, ss1752344764, ss1798560652, ss1917761390, ss1921331396, ss1946069753, ss1958517925, ss1969054731, ss2021213984, ss2149279980, ss2625107040, ss2633754724, ss2703932192, ss2787659739, ss2985203630, ss2985825020, ss2991551090, ss3022082471, ss3344796315, ss3628312977, ss3634817782, ss3640525081, ss3644772460, ss3652534604, ss3653971634, ss3659449227, ss3729477032, ss3744488732, ss3745117674, ss3758228706, ss3772614053, ss3784186852, ss3789720410, ss3794593860, ss3827567475, ss3837204094, ss3854844414, ss3900591996, ss3984499814, ss3984961225, ss5157034660, ss5314817146, ss5336794075, ss5506835932, ss5624475318, ss5631189387, ss5821754112, ss5847207645, ss5847907574, ss5957454146, ss5979603980	NC_000002.11:233998480:C:A	NC_000002.12:233133770:C:A	(self)
17520788, 94330318, 2034040, 6703476, 217352, 21916874, 352500285, 7075819284, ss2240125974, ss3024367149, ss3706257297, ss3725884247, ss3770995883, ss3802591471, ss3842626739, ss3950325475, ss4548677406, ss5252446728, ss5452016995, ss5529994853, ss5688079770, ss5803323702, ss5852999477, ss5935181818	NC_000002.12:233133770:C:A	NC_000002.12:233133770:C:A	(self)
ss16834325, ss17647740, ss21691686	NT_005403.14:84207892:C:A	NC_000002.12:233133770:C:A	(self)
ss44282684, ss65816914, ss103698241, ss138650940, ss154863779, ss161244669, ss410890287	NT_005403.17:84207898:C:A	NC_000002.12:233133770:C:A	(self)
7075819284	NC_000002.12:233133770:C:G	NC_000002.12:233133770:C:G	(self)
7769390, ss3900591996	NC_000002.11:233998480:C:T	NC_000002.12:233133770:C:T	(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 rs10933436

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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs10933436