Name: rs3836707
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.

rs3836707

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:119528054-119528063 (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: delAA / delA / dupA / dupAA / dupA…
delAA / delA / dupA / dupAA / dupAAA
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.3074 (1919/6242, ALFA)
(A)₁₀=0.4949 (1891/3821, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PDE5A : 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	6242	AAAAAAAAAA=0.5138	AAAAAAAAA=0.3074, AAAAAAAAAAA=0.1788, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000	0.521922	0.189366	0.288713	32
European	Sub	5326	AAAAAAAAAA=0.4311	AAAAAAAAA=0.3597, AAAAAAAAAAA=0.2092, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000	0.393957	0.240521	0.365521	32
African	Sub	710	AAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	38	AAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	672	AAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	6	AAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	6	AAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAAAAAAAAA=0	AAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	18	AAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	84	AAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	12	AAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	86	AAAAAAAAAA=0.94	AAAAAAAAA=0.03, AAAAAAAAAAA=0.02, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00	0.95122	0.0	0.04878	0

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	6242	(A)₁₀=0.5138	delA=0.3074, dupA=0.1788, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	European	Sub	5326	(A)₁₀=0.4311	delA=0.3597, dupA=0.2092, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	African	Sub	710	(A)₁₀=1.000	delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Other	Sub	86	(A)₁₀=0.94	delA=0.03, dupA=0.02, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Latin American 2	Sub	84	(A)₁₀=1.00	delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	18	(A)₁₀=1.00	delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	South Asian	Sub	12	(A)₁₀=1.00	delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Asian	Sub	6	(A)₁₀=1.0	delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0
1000Genomes	Global	Study-wide	3821	(A)₁₀=0.4949	delA=0.5051
1000Genomes	African	Sub	1105	(A)₁₀=0.6054	delA=0.3946
1000Genomes	Europe	Sub	802	(A)₁₀=0.414	delA=0.586
1000Genomes	East Asian	Sub	711	(A)₁₀=0.352	delA=0.648
1000Genomes	South Asian	Sub	658	(A)₁₀=0.571	delA=0.429
1000Genomes	American	Sub	545	(A)₁₀=0.484	delA=0.516

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 4	NC_000004.12:g.119528062_119528063del
GRCh38.p14 chr 4	NC_000004.12:g.119528063del
GRCh38.p14 chr 4	NC_000004.12:g.119528063dup
GRCh38.p14 chr 4	NC_000004.12:g.119528062_119528063dup
GRCh38.p14 chr 4	NC_000004.12:g.119528061_119528063dup
GRCh37.p13 chr 4	NC_000004.11:g.120449217_120449218del
GRCh37.p13 chr 4	NC_000004.11:g.120449218del
GRCh37.p13 chr 4	NC_000004.11:g.120449218dup
GRCh37.p13 chr 4	NC_000004.11:g.120449217_120449218dup
GRCh37.p13 chr 4	NC_000004.11:g.120449216_120449218dup

Gene: PDE5A, phosphodiesterase 5A (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PDE5A transcript variant 1	NM_001083.4:c.1633-2360_1… NM_001083.4:c.1633-2360_1633-2359del	N/A	Intron Variant
PDE5A transcript variant 2	NM_033430.3:c.1507-2360_1… NM_033430.3:c.1507-2360_1507-2359del	N/A	Intron Variant
PDE5A transcript variant 3	NM_033437.4:c.1477-2360_1… NM_033437.4:c.1477-2360_1477-2359del	N/A	Intron Variant
PDE5A transcript variant X1	XM_017008791.3:c.1633-236… XM_017008791.3:c.1633-2360_1633-2359del	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	(A)₁₀=	delAA	delA	dupA	dupAA	dupAAA
GRCh38.p14 chr 4	NC_000004.12:g.119528054_119528063=	NC_000004.12:g.119528062_119528063del	NC_000004.12:g.119528063del	NC_000004.12:g.119528063dup	NC_000004.12:g.119528062_119528063dup	NC_000004.12:g.119528061_119528063dup
GRCh37.p13 chr 4	NC_000004.11:g.120449209_120449218=	NC_000004.11:g.120449217_120449218del	NC_000004.11:g.120449218del	NC_000004.11:g.120449218dup	NC_000004.11:g.120449217_120449218dup	NC_000004.11:g.120449216_120449218dup
PDE5A transcript variant 1	NM_001083.3:c.1633-2359=	NM_001083.3:c.1633-2360_1633-2359del	NM_001083.3:c.1633-2359del	NM_001083.3:c.1633-2359dup	NM_001083.3:c.1633-2360_1633-2359dup	NM_001083.3:c.1633-2361_1633-2359dup
PDE5A transcript variant 1	NM_001083.4:c.1633-2359=	NM_001083.4:c.1633-2360_1633-2359del	NM_001083.4:c.1633-2359del	NM_001083.4:c.1633-2359dup	NM_001083.4:c.1633-2360_1633-2359dup	NM_001083.4:c.1633-2361_1633-2359dup
PDE5A transcript variant 2	NM_033430.2:c.1507-2359=	NM_033430.2:c.1507-2360_1507-2359del	NM_033430.2:c.1507-2359del	NM_033430.2:c.1507-2359dup	NM_033430.2:c.1507-2360_1507-2359dup	NM_033430.2:c.1507-2361_1507-2359dup
PDE5A transcript variant 2	NM_033430.3:c.1507-2359=	NM_033430.3:c.1507-2360_1507-2359del	NM_033430.3:c.1507-2359del	NM_033430.3:c.1507-2359dup	NM_033430.3:c.1507-2360_1507-2359dup	NM_033430.3:c.1507-2361_1507-2359dup
PDE5A transcript variant 3	NM_033437.3:c.1477-2359=	NM_033437.3:c.1477-2360_1477-2359del	NM_033437.3:c.1477-2359del	NM_033437.3:c.1477-2359dup	NM_033437.3:c.1477-2360_1477-2359dup	NM_033437.3:c.1477-2361_1477-2359dup
PDE5A transcript variant 3	NM_033437.4:c.1477-2359=	NM_033437.4:c.1477-2360_1477-2359del	NM_033437.4:c.1477-2359del	NM_033437.4:c.1477-2359dup	NM_033437.4:c.1477-2360_1477-2359dup	NM_033437.4:c.1477-2361_1477-2359dup
PDE5A transcript variant X1	XM_017008791.3:c.1633-2359=	XM_017008791.3:c.1633-2360_1633-2359del	XM_017008791.3:c.1633-2359del	XM_017008791.3:c.1633-2359dup	XM_017008791.3:c.1633-2360_1633-2359dup	XM_017008791.3:c.1633-2361_1633-2359dup

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#.

61 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	YUSUKE	ss5023220	Dec 03, 2013 (138)
2	HUMANGENOME_JCVI	ss95367189	Feb 03, 2009 (130)
3	GMI	ss287755921	May 09, 2011 (137)
4	GMI	ss288574447	May 04, 2012 (137)
5	GMI	ss288574448	May 04, 2012 (138)
6	PJP	ss295184989	May 09, 2011 (137)
7	PJP	ss295184990	May 09, 2011 (134)
8	1000GENOMES	ss326566798	May 09, 2011 (134)
9	1000GENOMES	ss326601596	Jan 10, 2018 (151)
10	1000GENOMES	ss326782384	May 09, 2011 (134)
11	LUNTER	ss551408313	Apr 25, 2013 (138)
12	LUNTER	ss551539191	Apr 25, 2013 (138)
13	LUNTER	ss553160242	Apr 25, 2013 (138)
14	SSMP	ss663451057	Apr 01, 2015 (144)
15	BILGI_BIOE	ss666275494	Apr 25, 2013 (138)
16	1000GENOMES	ss1372708382	Aug 21, 2014 (142)
17	1000GENOMES	ss1372708385	Aug 21, 2014 (142)
18	DDI	ss1536425524	Apr 01, 2015 (144)
19	EVA_UK10K_ALSPAC	ss1704330874	Apr 01, 2015 (144)
20	EVA_UK10K_TWINSUK	ss1704331728	Apr 01, 2015 (144)
21	EVA_UK10K_TWINSUK	ss1710166281	Apr 01, 2015 (144)
22	EVA_UK10K_ALSPAC	ss1710166283	Apr 01, 2015 (144)
23	HAMMER_LAB	ss1802099439	Sep 08, 2015 (146)
24	SWEGEN	ss2995438526	Nov 08, 2017 (151)
25	MCHAISSO	ss3064120108	Nov 08, 2017 (151)
26	MCHAISSO	ss3064987707	Nov 08, 2017 (151)
27	BEROUKHIMLAB	ss3644163670	Oct 12, 2018 (152)
28	BIOINF_KMB_FNS_UNIBA	ss3645822184	Oct 12, 2018 (152)
29	BIOINF_KMB_FNS_UNIBA	ss3645822185	Oct 12, 2018 (152)
30	URBANLAB	ss3647832508	Oct 12, 2018 (152)
31	EVA_DECODE	ss3712925566	Jul 13, 2019 (153)
32	EVA_DECODE	ss3712925567	Jul 13, 2019 (153)
33	PACBIO	ss3784839773	Jul 13, 2019 (153)
34	PACBIO	ss3790278703	Jul 13, 2019 (153)
35	PACBIO	ss3795154136	Jul 13, 2019 (153)
36	KHV_HUMAN_GENOMES	ss3805480615	Jul 13, 2019 (153)
37	KHV_HUMAN_GENOMES	ss3805480616	Jul 13, 2019 (153)
38	KHV_HUMAN_GENOMES	ss3805480617	Jul 13, 2019 (153)
39	EVA	ss3828771524	Apr 26, 2020 (154)
40	EVA	ss3837829917	Apr 26, 2020 (154)
41	EVA	ss3843268986	Apr 26, 2020 (154)
42	KOGIC	ss3954991468	Apr 26, 2020 (154)
43	KOGIC	ss3954991469	Apr 26, 2020 (154)
44	KOGIC	ss3954991470	Apr 26, 2020 (154)
45	GNOMAD	ss4119175634	Apr 26, 2021 (155)
46	GNOMAD	ss4119175635	Apr 26, 2021 (155)
47	GNOMAD	ss4119175636	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5167688318	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5167688319	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5167688320	Apr 26, 2021 (155)
51	1000G_HIGH_COVERAGE	ss5260773751	Oct 13, 2022 (156)
52	1000G_HIGH_COVERAGE	ss5260773752	Oct 13, 2022 (156)
53	1000G_HIGH_COVERAGE	ss5260773753	Oct 13, 2022 (156)
54	1000G_HIGH_COVERAGE	ss5260773754	Oct 13, 2022 (156)
55	HUGCELL_USP	ss5459357987	Oct 13, 2022 (156)
56	HUGCELL_USP	ss5459357988	Oct 13, 2022 (156)
57	TOMMO_GENOMICS	ss5702591775	Oct 13, 2022 (156)
58	TOMMO_GENOMICS	ss5702591776	Oct 13, 2022 (156)
59	TOMMO_GENOMICS	ss5702591777	Oct 13, 2022 (156)
60	EVA	ss5844613437	Oct 13, 2022 (156)
61	EVA	ss5844613438	Oct 13, 2022 (156)
62	1000Genomes	NC_000004.11 - 120449209	Oct 12, 2018 (152)
63	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 12791919 (NC_000004.11:120449208::A 719/3854) Row 12791920 (NC_000004.11:120449208:A: 1828/3854)	-	Oct 12, 2018 (152)
64	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 12791919 (NC_000004.11:120449208::A 719/3854) Row 12791920 (NC_000004.11:120449208:A: 1828/3854)	-	Oct 12, 2018 (152)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 162905979 (NC_000004.12:119528053::A 27740/137704) Row 162905980 (NC_000004.12:119528053::AA 233/137854) Row 162905981 (NC_000004.12:119528053::AAA 1/137860)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 162905979 (NC_000004.12:119528053::A 27740/137704) Row 162905980 (NC_000004.12:119528053::AA 233/137854) Row 162905981 (NC_000004.12:119528053::AAA 1/137860)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 162905979 (NC_000004.12:119528053::A 27740/137704) Row 162905980 (NC_000004.12:119528053::AA 233/137854) Row 162905981 (NC_000004.12:119528053::AAA 1/137860)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 162905979 (NC_000004.12:119528053::A 27740/137704) Row 162905980 (NC_000004.12:119528053::AA 233/137854) Row 162905981 (NC_000004.12:119528053::AAA 1/137860)...	-	Apr 26, 2021 (155)
69	Korean Genome Project Submission ignored due to conflicting rows: Row 11369469 (NC_000004.12:119528054::A 666/1832) Row 11369470 (NC_000004.12:119528053:A: 734/1832) Row 11369471 (NC_000004.12:119528054::AA 20/1832)	-	Apr 26, 2020 (154)
70	Korean Genome Project Submission ignored due to conflicting rows: Row 11369469 (NC_000004.12:119528054::A 666/1832) Row 11369470 (NC_000004.12:119528053:A: 734/1832) Row 11369471 (NC_000004.12:119528054::AA 20/1832)	-	Apr 26, 2020 (154)
71	Korean Genome Project Submission ignored due to conflicting rows: Row 11369469 (NC_000004.12:119528054::A 666/1832) Row 11369470 (NC_000004.12:119528053:A: 734/1832) Row 11369471 (NC_000004.12:119528054::AA 20/1832)	-	Apr 26, 2020 (154)
72	8.3KJPN Submission ignored due to conflicting rows: Row 25657625 (NC_000004.11:120449208::A 6274/16760) Row 25657626 (NC_000004.11:120449208:A: 7646/16760) Row 25657627 (NC_000004.11:120449208::AA 102/16760)	-	Apr 26, 2021 (155)
73	8.3KJPN Submission ignored due to conflicting rows: Row 25657625 (NC_000004.11:120449208::A 6274/16760) Row 25657626 (NC_000004.11:120449208:A: 7646/16760) Row 25657627 (NC_000004.11:120449208::AA 102/16760)	-	Apr 26, 2021 (155)
74	8.3KJPN Submission ignored due to conflicting rows: Row 25657625 (NC_000004.11:120449208::A 6274/16760) Row 25657626 (NC_000004.11:120449208:A: 7646/16760) Row 25657627 (NC_000004.11:120449208::AA 102/16760)	-	Apr 26, 2021 (155)
75	14KJPN Submission ignored due to conflicting rows: Row 36428879 (NC_000004.12:119528053:A: 12867/28258) Row 36428880 (NC_000004.12:119528053::A 10686/28258) Row 36428881 (NC_000004.12:119528053::AA 178/28258)	-	Oct 13, 2022 (156)
76	14KJPN Submission ignored due to conflicting rows: Row 36428879 (NC_000004.12:119528053:A: 12867/28258) Row 36428880 (NC_000004.12:119528053::A 10686/28258) Row 36428881 (NC_000004.12:119528053::AA 178/28258)	-	Oct 13, 2022 (156)
77	14KJPN Submission ignored due to conflicting rows: Row 36428879 (NC_000004.12:119528053:A: 12867/28258) Row 36428880 (NC_000004.12:119528053::A 10686/28258) Row 36428881 (NC_000004.12:119528053::AA 178/28258)	-	Oct 13, 2022 (156)
78	UK 10K study - Twins Submission ignored due to conflicting rows: Row 12791919 (NC_000004.11:120449208::A 778/3708) Row 12791920 (NC_000004.11:120449208:A: 1787/3708)	-	Oct 12, 2018 (152)
79	UK 10K study - Twins Submission ignored due to conflicting rows: Row 12791919 (NC_000004.11:120449208::A 778/3708) Row 12791920 (NC_000004.11:120449208:A: 1787/3708)	-	Oct 12, 2018 (152)
80	ALFA	NC_000004.12 - 119528054	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)
rs11289914	May 11, 2012 (137)
rs34578192	May 23, 2006 (127)
rs373299874	May 13, 2013 (138)
rs201793085	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5260773754	NC_000004.12:119528053:AA:	NC_000004.12:119528053:AAAAAAAAAA:… NC_000004.12:119528053:AAAAAAAAAA:AAAAAAAA
ss288574447, ss295184989, ss326601596, ss551408313	NC_000004.10:120668656:A:	NC_000004.12:119528053:AAAAAAAAAA:… NC_000004.12:119528053:AAAAAAAAAA:AAAAAAAAA	(self)
ss295184990	NC_000004.10:120668665:A:	NC_000004.12:119528053:AAAAAAAAAA:… NC_000004.12:119528053:AAAAAAAAAA:AAAAAAAAA	(self)
22994848, ss663451057, ss666275494, ss1372708382, ss1536425524, ss1704330874, ss1704331728, ss2995438526, ss3644163670, ss3837829917, ss5167688319, ss5844613437	NC_000004.11:120449208:A:	NC_000004.12:119528053:AAAAAAAAAA:… NC_000004.12:119528053:AAAAAAAAAA:AAAAAAAAA	(self)
ss3064120108, ss3064987707, ss3645822184, ss3647832508, ss3712925567, ss3805480615, ss3843268986, ss3954991469, ss5260773751, ss5459357987, ss5702591775	NC_000004.12:119528053:A:	NC_000004.12:119528053:AAAAAAAAAA:… NC_000004.12:119528053:AAAAAAAAAA:AAAAAAAAA	(self)
9043562088	NC_000004.12:119528053:AAAAAAAAAA:… NC_000004.12:119528053:AAAAAAAAAA:AAAAAAAAA	NC_000004.12:119528053:AAAAAAAAAA:… NC_000004.12:119528053:AAAAAAAAAA:AAAAAAAAA	(self)
ss287755921	NT_016354.19:44996929:A:	NC_000004.12:119528053:AAAAAAAAAA:… NC_000004.12:119528053:AAAAAAAAAA:AAAAAAAAA	(self)
ss5023220, ss95367189	NT_016354.19:44996938:A:	NC_000004.12:119528053:AAAAAAAAAA:… NC_000004.12:119528053:AAAAAAAAAA:AAAAAAAAA	(self)
ss326566798, ss326782384, ss551539191, ss553160242	NC_000004.10:120668656::A	NC_000004.12:119528053:AAAAAAAAAA:… NC_000004.12:119528053:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss288574448	NC_000004.10:120668666::A	NC_000004.12:119528053:AAAAAAAAAA:… NC_000004.12:119528053:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss1802099439, ss3784839773, ss3790278703, ss3795154136, ss3828771524, ss5167688318, ss5844613438	NC_000004.11:120449208::A	NC_000004.12:119528053:AAAAAAAAAA:… NC_000004.12:119528053:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss1372708385, ss1710166281, ss1710166283	NC_000004.11:120449209::A	NC_000004.12:119528053:AAAAAAAAAA:… NC_000004.12:119528053:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss3645822185, ss3805480616, ss4119175634, ss5260773752, ss5459357988, ss5702591776	NC_000004.12:119528053::A	NC_000004.12:119528053:AAAAAAAAAA:… NC_000004.12:119528053:AAAAAAAAAA:AAAAAAAAAAA	(self)
9043562088	NC_000004.12:119528053:AAAAAAAAAA:… NC_000004.12:119528053:AAAAAAAAAA:AAAAAAAAAAA	NC_000004.12:119528053:AAAAAAAAAA:… NC_000004.12:119528053:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss3712925566, ss3805480617, ss3954991468	NC_000004.12:119528054::A	NC_000004.12:119528053:AAAAAAAAAA:… NC_000004.12:119528053:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss5167688320	NC_000004.11:120449208::AA	NC_000004.12:119528053:AAAAAAAAAA:… NC_000004.12:119528053:AAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4119175635, ss5260773753, ss5702591777	NC_000004.12:119528053::AA	NC_000004.12:119528053:AAAAAAAAAA:… NC_000004.12:119528053:AAAAAAAAAA:AAAAAAAAAAAA	(self)
9043562088	NC_000004.12:119528053:AAAAAAAAAA:… NC_000004.12:119528053:AAAAAAAAAA:AAAAAAAAAAAA	NC_000004.12:119528053:AAAAAAAAAA:… NC_000004.12:119528053:AAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3954991470	NC_000004.12:119528054::AA	NC_000004.12:119528053:AAAAAAAAAA:… NC_000004.12:119528053:AAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4119175636	NC_000004.12:119528053::AAA	NC_000004.12:119528053:AAAAAAAAAA:… NC_000004.12:119528053:AAAAAAAAAA:AAAAAAAAAAAAA	(self)
9043562088	NC_000004.12:119528053:AAAAAAAAAA:… NC_000004.12:119528053:AAAAAAAAAA:AAAAAAAAAAAAA	NC_000004.12:119528053:AAAAAAAAAA:… NC_000004.12:119528053:AAAAAAAAAA:AAAAAAAAAAAAA	(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 rs3836707

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

rs3836707