Name: rs3922435
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.

rs3922435

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr13:30740543 (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: T>A / T>C
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.052847 (13988/264690, TOPMED)
T=0.00000 (0/28258, 14KJPN)
T=0.00000 (0/16760, 8.3KJPN) (+ 19 more)
T=0.0372 (318/8546, ALFA)
T=0.0529 (339/6404, 1000G_30x)
T=0.0507 (254/5008, 1000G)
T=0.0071 (32/4480, Estonian)
T=0.0138 (53/3854, ALSPAC)
T=0.0100 (37/3708, TWINSUK)
T=0.0000 (0/2930, KOREAN)
A=0.0000 (0/2930, KOREAN)
T=0.0000 (0/1832, Korea1K)
T=0.0212 (24/1130, Daghestan)
T=0.007 (7/998, GoNL)
T=0.000 (0/792, PRJEB37584)
T=0.010 (6/600, NorthernSweden)
T=0.022 (12/552, SGDP_PRJ)
T=0.055 (18/330, HapMap)
T=0.046 (10/216, Qatari)
T=0.000 (0/212, Vietnamese)
T=0.07 (4/56, Ancient Sardinia)
T=0.00 (0/56, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ALOX5AP : Intron Variant
LOC124903146 : 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	8546	T=0.0372	A=0.0000, C=0.9628
European	Sub	6678	T=0.0094	A=0.0000, C=0.9906
African	Sub	1328	T=0.1815	A=0.0000, C=0.8185
African Others	Sub	38	T=0.16	A=0.00, C=0.84
African American	Sub	1290	T=0.1822	A=0.0000, C=0.8178
Asian	Sub	8	T=0.0	A=0.0, C=1.0
East Asian	Sub	4	T=0.0	A=0.0, C=1.0
Other Asian	Sub	4	T=0.0	A=0.0, C=1.0
Latin American 1	Sub	8	T=0.1	A=0.0, C=0.9
Latin American 2	Sub	6	T=0.0	A=0.0, C=1.0
South Asian	Sub	4	T=0.0	A=0.0, C=1.0
Other	Sub	514	T=0.025	A=0.000, C=0.975

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	T=0.052847	C=0.947153
14KJPN	JAPANESE	Study-wide	28258	T=0.00000	C=1.00000
8.3KJPN	JAPANESE	Study-wide	16760	T=0.00000	C=1.00000
Allele Frequency Aggregator	Total	Global	8546	T=0.0372	A=0.0000, C=0.9628
Allele Frequency Aggregator	European	Sub	6678	T=0.0094	A=0.0000, C=0.9906
Allele Frequency Aggregator	African	Sub	1328	T=0.1815	A=0.0000, C=0.8185
Allele Frequency Aggregator	Other	Sub	514	T=0.025	A=0.000, C=0.975
Allele Frequency Aggregator	Latin American 1	Sub	8	T=0.1	A=0.0, C=0.9
Allele Frequency Aggregator	Asian	Sub	8	T=0.0	A=0.0, C=1.0
Allele Frequency Aggregator	Latin American 2	Sub	6	T=0.0	A=0.0, C=1.0
Allele Frequency Aggregator	South Asian	Sub	4	T=0.0	A=0.0, C=1.0
1000Genomes_30x	Global	Study-wide	6404	T=0.0529	C=0.9471
1000Genomes_30x	African	Sub	1786	T=0.1697	C=0.8303
1000Genomes_30x	Europe	Sub	1266	T=0.0118	C=0.9882
1000Genomes_30x	South Asian	Sub	1202	T=0.0058	C=0.9942
1000Genomes_30x	East Asian	Sub	1170	T=0.0000	C=1.0000
1000Genomes_30x	American	Sub	980	T=0.014	C=0.986
1000Genomes	Global	Study-wide	5008	T=0.0507	C=0.9493
1000Genomes	African	Sub	1322	T=0.1710	C=0.8290
1000Genomes	East Asian	Sub	1008	T=0.0000	C=1.0000
1000Genomes	Europe	Sub	1006	T=0.0119	C=0.9881
1000Genomes	South Asian	Sub	978	T=0.005	C=0.995
1000Genomes	American	Sub	694	T=0.016	C=0.984
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.0071	C=0.9929
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.0138	C=0.9862
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.0100	C=0.9900
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.0000	A=0.0000, C=1.0000
Korean Genome Project	KOREAN	Study-wide	1832	T=0.0000	C=1.0000
Genome-wide autozygosity in Daghestan	Global	Study-wide	1130	T=0.0212	C=0.9788
Genome-wide autozygosity in Daghestan	Daghestan	Sub	626	T=0.019	C=0.981
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	T=0.035	C=0.965
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	T=0.016	C=0.984
Genome-wide autozygosity in Daghestan	Europe	Sub	108	T=0.028	C=0.972
Genome-wide autozygosity in Daghestan	South Asian	Sub	94	T=0.00	C=1.00
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	T=0.06	C=0.94
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.007	C=0.993
CNV burdens in cranial meningiomas	Global	Study-wide	792	T=0.000	C=1.000
CNV burdens in cranial meningiomas	CRM	Sub	792	T=0.000	C=1.000
Northern Sweden	ACPOP	Study-wide	600	T=0.010	C=0.990
SGDP_PRJ	Global	Study-wide	552	T=0.022	C=0.978
HapMap	Global	Study-wide	330	T=0.055	C=0.945
HapMap	African	Sub	120	T=0.142	C=0.858
HapMap	American	Sub	120	T=0.008	C=0.992
HapMap	Asian	Sub	90	T=0.00	C=1.00
Qatari	Global	Study-wide	216	T=0.046	C=0.954
A Vietnamese Genetic Variation Database	Global	Study-wide	212	T=0.000	C=1.000
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	56	T=0.07	C=0.93
Siberian	Global	Study-wide	56	T=0.00	C=1.00

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 13	NC_000013.11:g.30740543T>A
GRCh38.p14 chr 13	NC_000013.11:g.30740543T>C
GRCh37.p13 chr 13	NC_000013.10:g.31314680T>A
GRCh37.p13 chr 13	NC_000013.10:g.31314680T>C
ALOX5AP RefSeqGene	NG_011963.2:g.32066T>A
ALOX5AP RefSeqGene	NG_011963.2:g.32066T>C

Gene: ALOX5AP, arachidonate 5-lipoxygenase activating protein (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ALOX5AP transcript variant 2	NM_001204406.2:c.242-3517… NM_001204406.2:c.242-3517T>A	N/A	Intron Variant
ALOX5AP transcript variant 1	NM_001629.4:c.71-3517T>A	N/A	Intron Variant
ALOX5AP transcript variant X1	XM_017020522.3:c.	N/A	Genic Upstream Transcript Variant

Gene: LOC124903146, uncharacterized LOC124903146 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC124903146 transcript	XR_007063743.1:n.	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	T=	A	C
GRCh38.p14 chr 13	NC_000013.11:g.30740543=	NC_000013.11:g.30740543T>A	NC_000013.11:g.30740543T>C
GRCh37.p13 chr 13	NC_000013.10:g.31314680=	NC_000013.10:g.31314680T>A	NC_000013.10:g.31314680T>C
ALOX5AP RefSeqGene	NG_011963.2:g.32066=	NG_011963.2:g.32066T>A	NG_011963.2:g.32066T>C
ALOX5AP transcript variant 2	NM_001204406.1:c.242-3517=	NM_001204406.1:c.242-3517T>A	NM_001204406.1:c.242-3517T>C
ALOX5AP transcript variant 2	NM_001204406.2:c.242-3517=	NM_001204406.2:c.242-3517T>A	NM_001204406.2:c.242-3517T>C
ALOX5AP transcript variant 1	NM_001629.3:c.71-3517=	NM_001629.3:c.71-3517T>A	NM_001629.3:c.71-3517T>C
ALOX5AP transcript variant 1	NM_001629.4:c.71-3517=	NM_001629.4:c.71-3517T>A	NM_001629.4:c.71-3517T>C

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#.

96 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss5153344	Oct 10, 2002 (108)
2	SC_JCM	ss5661805	Feb 20, 2003 (111)
3	WI_SSAHASNP	ss6580031	Feb 20, 2003 (111)
4	SC_SNP	ss13163561	Dec 05, 2003 (119)
5	BCM_SSAHASNP	ss14158677	Dec 05, 2003 (119)
6	CSHL-HAPMAP	ss16616952	Feb 27, 2004 (120)
7	SSAHASNP	ss21146500	Apr 05, 2004 (121)
8	PGA-UW-FHCRC	ss23143238	Sep 20, 2004 (126)
9	ABI	ss43448468	Mar 10, 2006 (126)
10	PGA-UW-FHCRC	ss52086109	Oct 16, 2006 (127)
11	HGSV	ss78388268	Dec 07, 2007 (129)
12	HGSV	ss79005262	Dec 07, 2007 (129)
13	HGSV	ss83131159	Dec 15, 2007 (130)
14	HGSV	ss83433870	Dec 15, 2007 (130)
15	HGSV	ss85597817	Dec 15, 2007 (130)
16	BCMHGSC_JDW	ss89570174	Mar 24, 2008 (129)
17	HUMANGENOME_JCVI	ss96956311	Feb 06, 2009 (130)
18	BGI	ss106323762	Feb 06, 2009 (130)
19	1000GENOMES	ss112661771	Jan 25, 2009 (130)
20	1000GENOMES	ss114490985	Jan 25, 2009 (130)
21	ILLUMINA-UK	ss118408126	Feb 14, 2009 (130)
22	ENSEMBL	ss133513826	Dec 01, 2009 (131)
23	ENSEMBL	ss137267998	Dec 01, 2009 (131)
24	GMI	ss154609816	Dec 01, 2009 (131)
25	COMPLETE_GENOMICS	ss167828748	Jul 04, 2010 (132)
26	COMPLETE_GENOMICS	ss169121252	Jul 04, 2010 (132)
27	COMPLETE_GENOMICS	ss170959683	Jul 04, 2010 (132)
28	ILLUMINA	ss173673604	Jul 04, 2010 (132)
29	BUSHMAN	ss199035067	Jul 04, 2010 (132)
30	BCM-HGSC-SUB	ss208488165	Jul 04, 2010 (132)
31	1000GENOMES	ss226108792	Jul 14, 2010 (132)
32	1000GENOMES	ss236197538	Jul 15, 2010 (132)
33	1000GENOMES	ss242703302	Jul 15, 2010 (132)
34	ILLUMINA	ss244298511	Jul 04, 2010 (132)
35	BL	ss254900428	May 09, 2011 (134)
36	GMI	ss281659517	May 04, 2012 (137)
37	GMI	ss286678832	Apr 25, 2013 (138)
38	PJP	ss291568830	May 09, 2011 (134)
39	ILLUMINA	ss535550514	Sep 08, 2015 (146)
40	TISHKOFF	ss563582502	Apr 25, 2013 (138)
41	SSMP	ss659178506	Apr 25, 2013 (138)
42	EVA-GONL	ss990245596	Aug 21, 2014 (142)
43	JMKIDD_LAB	ss1078976658	Aug 21, 2014 (142)
44	1000GENOMES	ss1347682153	Aug 21, 2014 (142)
45	HAMMER_LAB	ss1397653698	Sep 08, 2015 (146)
46	DDI	ss1427145937	Apr 01, 2015 (144)
47	EVA_UK10K_ALSPAC	ss1629991641	Apr 01, 2015 (144)
48	EVA_DECODE	ss1642350111	Apr 01, 2015 (144)
49	EVA_UK10K_TWINSUK	ss1672985674	Apr 01, 2015 (144)
50	HAMMER_LAB	ss1807549305	Sep 08, 2015 (146)
51	WEILL_CORNELL_DGM	ss1933614770	Feb 12, 2016 (147)
52	GENOMED	ss1967747862	Jul 19, 2016 (147)
53	JJLAB	ss2027564068	Sep 14, 2016 (149)
54	USC_VALOUEV	ss2155928769	Dec 20, 2016 (150)
55	HUMAN_LONGEVITY	ss2195227922	Dec 20, 2016 (150)
56	SYSTEMSBIOZJU	ss2628269916	Nov 08, 2017 (151)
57	GRF	ss2700301017	Nov 08, 2017 (151)
58	GNOMAD	ss2918117279	Nov 08, 2017 (151)
59	SWEGEN	ss3010799950	Nov 08, 2017 (151)
60	BIOINF_KMB_FNS_UNIBA	ss3027597977	Nov 08, 2017 (151)
61	CSHL	ss3350390173	Nov 08, 2017 (151)
62	ILLUMINA	ss3627033529	Oct 12, 2018 (152)
63	ILLUMINA	ss3638003188	Oct 12, 2018 (152)
64	URBANLAB	ss3650001148	Oct 12, 2018 (152)
65	EGCUT_WGS	ss3678060329	Jul 13, 2019 (153)
66	EVA_DECODE	ss3695022979	Jul 13, 2019 (153)
67	ACPOP	ss3739626824	Jul 13, 2019 (153)
68	EVA	ss3751295857	Jul 13, 2019 (153)
69	PACBIO	ss3787419417	Jul 13, 2019 (153)
70	PACBIO	ss3792491515	Jul 13, 2019 (153)
71	PACBIO	ss3797375266	Jul 13, 2019 (153)
72	KHV_HUMAN_GENOMES	ss3816626840	Jul 13, 2019 (153)
73	EVA	ss3833476070	Apr 27, 2020 (154)
74	EVA	ss3840315533	Apr 27, 2020 (154)
75	EVA	ss3845800415	Apr 27, 2020 (154)
76	SGDP_PRJ	ss3879693686	Apr 27, 2020 (154)
77	KRGDB	ss3928518080	Apr 27, 2020 (154)
78	KOGIC	ss3973299227	Apr 27, 2020 (154)
79	EVA	ss3984678056	Apr 26, 2021 (155)
80	EVA	ss3985632097	Apr 26, 2021 (155)
81	TOPMED	ss4941530373	Apr 26, 2021 (155)
82	TOMMO_GENOMICS	ss5209385671	Apr 26, 2021 (155)
83	1000G_HIGH_COVERAGE	ss5293263415	Oct 16, 2022 (156)
84	EVA	ss5409904791	Oct 16, 2022 (156)
85	HUGCELL_USP	ss5487673678	Oct 16, 2022 (156)
86	EVA	ss5510924504	Oct 16, 2022 (156)
87	1000G_HIGH_COVERAGE	ss5591973566	Oct 16, 2022 (156)
88	SANFORD_IMAGENETICS	ss5624320699	Oct 16, 2022 (156)
89	SANFORD_IMAGENETICS	ss5654498127	Oct 16, 2022 (156)
90	TOMMO_GENOMICS	ss5761087122	Oct 16, 2022 (156)
91	YY_MCH	ss5813992757	Oct 16, 2022 (156)
92	EVA	ss5839288459	Oct 16, 2022 (156)
93	EVA	ss5850668450	Oct 16, 2022 (156)
94	EVA	ss5924560839	Oct 16, 2022 (156)
95	EVA	ss5945905867	Oct 16, 2022 (156)
96	EVA	ss5980783581	Oct 16, 2022 (156)
97	1000Genomes	NC_000013.10 - 31314680	Oct 12, 2018 (152)
98	1000Genomes_30x	NC_000013.11 - 30740543	Oct 16, 2022 (156)
99	The Avon Longitudinal Study of Parents and Children	NC_000013.10 - 31314680	Oct 12, 2018 (152)
100	Genome-wide autozygosity in Daghestan	NC_000013.9 - 30212680	Apr 27, 2020 (154)
101	Genetic variation in the Estonian population	NC_000013.10 - 31314680	Oct 12, 2018 (152)
102	gnomAD - Genomes Submission ignored due to conflicting rows: Row 426826660 (NC_000013.11:30740542:T:A 1/140250) Row 426826661 (NC_000013.11:30740542:T:C 133019/140226)	-	Apr 26, 2021 (155)
103	gnomAD - Genomes Submission ignored due to conflicting rows: Row 426826660 (NC_000013.11:30740542:T:A 1/140250) Row 426826661 (NC_000013.11:30740542:T:C 133019/140226)	-	Apr 26, 2021 (155)
104	Genome of the Netherlands Release 5	NC_000013.10 - 31314680	Apr 27, 2020 (154)
105	HapMap	NC_000013.11 - 30740543	Apr 27, 2020 (154)
106	KOREAN population from KRGDB	NC_000013.10 - 31314680	Apr 27, 2020 (154)
107	Korean Genome Project	NC_000013.11 - 30740543	Apr 27, 2020 (154)
108	Northern Sweden	NC_000013.10 - 31314680	Jul 13, 2019 (153)
109	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000013.10 - 31314680	Apr 26, 2021 (155)
110	CNV burdens in cranial meningiomas	NC_000013.10 - 31314680	Apr 26, 2021 (155)
111	Qatari	NC_000013.10 - 31314680	Apr 27, 2020 (154)
112	SGDP_PRJ	NC_000013.10 - 31314680	Apr 27, 2020 (154)
113	Siberian	NC_000013.10 - 31314680	Apr 27, 2020 (154)
114	8.3KJPN	NC_000013.10 - 31314680	Apr 26, 2021 (155)
115	14KJPN	NC_000013.11 - 30740543	Oct 16, 2022 (156)
116	TopMed	NC_000013.11 - 30740543	Apr 26, 2021 (155)
117	UK 10K study - Twins	NC_000013.10 - 31314680	Oct 12, 2018 (152)
118	A Vietnamese Genetic Variation Database	NC_000013.10 - 31314680	Jul 13, 2019 (153)
119	ALFA	NC_000013.11 - 30740543	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)
rs17245057	Mar 10, 2006 (126)
rs61007125	May 26, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
35695474, ss3928518080	NC_000013.10:31314679:T:A	NC_000013.11:30740542:T:A	(self)
9550583220	NC_000013.11:30740542:T:A	NC_000013.11:30740542:T:A	(self)
124374, ss78388268, ss79005262, ss83131159, ss83433870, ss85597817, ss89570174, ss112661771, ss114490985, ss118408126, ss167828748, ss169121252, ss170959683, ss199035067, ss208488165, ss244298511, ss254900428, ss281659517, ss286678832, ss291568830, ss1397653698, ss1642350111	NC_000013.9:30212679:T:C	NC_000013.11:30740542:T:C	(self)
60532947, 33621995, 23798577, 15001642, 35695474, 12911689, 858024, 227556, 15656700, 31710666, 8445123, 67354978, 33621995, 7457702, ss226108792, ss236197538, ss242703302, ss535550514, ss563582502, ss659178506, ss990245596, ss1078976658, ss1347682153, ss1427145937, ss1629991641, ss1672985674, ss1807549305, ss1933614770, ss1967747862, ss2027564068, ss2155928769, ss2628269916, ss2700301017, ss2918117279, ss3010799950, ss3350390173, ss3627033529, ss3638003188, ss3678060329, ss3739626824, ss3751295857, ss3787419417, ss3792491515, ss3797375266, ss3833476070, ss3840315533, ss3879693686, ss3928518080, ss3984678056, ss3985632097, ss5209385671, ss5409904791, ss5510924504, ss5624320699, ss5654498127, ss5839288459, ss5945905867, ss5980783581	NC_000013.10:31314679:T:C	NC_000013.11:30740542:T:C	(self)
79499501, 958928, 29677228, 94924226, 157076031, 9550583220, ss2195227922, ss3027597977, ss3650001148, ss3695022979, ss3816626840, ss3845800415, ss3973299227, ss4941530373, ss5293263415, ss5487673678, ss5591973566, ss5761087122, ss5813992757, ss5850668450, ss5924560839	NC_000013.11:30740542:T:C	NC_000013.11:30740542:T:C	(self)
ss13163561	NT_009799.12:12294679:T:C	NC_000013.11:30740542:T:C	(self)
ss14158677, ss16616952, ss21146500	NT_024524.13:12294679:T:C	NC_000013.11:30740542:T:C	(self)
ss5153344, ss5661805, ss6580031, ss23143238, ss43448468, ss52086109, ss96956311, ss106323762, ss133513826, ss137267998, ss154609816, ss173673604	NT_024524.14:12294679:T:C	NC_000013.11:30740542:T:C	(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 rs3922435

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.
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

rs3922435