Name: rs531690396
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.

rs531690396

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:149384910-149384926 (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(T)₅ / del(T)₄ / delTTT / delTT…
del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.01065 (160/15030, ALFA)
delT=0.1204 (603/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: IL17B : 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	15030	TTTTTTTTTTTTTTTTT=0.98882	TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.01065, TTTTTTTTTTTTTTTTTT=0.00053	0.980019	0.001332	0.018649	32
European	Sub	11406	TTTTTTTTTTTTTTTTT=0.98527	TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.01403, TTTTTTTTTTTTTTTTTT=0.00070	0.973661	0.001756	0.024583	32
African	Sub	2320	TTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	90	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	2230	TTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	94	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	70	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	24	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	128	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	570	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	86	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	426	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	15030	(T)₁₇=0.98882	delTT=0.00000, delT=0.01065, dupT=0.00053
Allele Frequency Aggregator	European	Sub	11406	(T)₁₇=0.98527	delTT=0.00000, delT=0.01403, dupT=0.00070
Allele Frequency Aggregator	African	Sub	2320	(T)₁₇=1.0000	delTT=0.0000, delT=0.0000, dupT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	570	(T)₁₇=1.000	delTT=0.000, delT=0.000, dupT=0.000
Allele Frequency Aggregator	Other	Sub	426	(T)₁₇=1.000	delTT=0.000, delT=0.000, dupT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	128	(T)₁₇=1.000	delTT=0.000, delT=0.000, dupT=0.000
Allele Frequency Aggregator	Asian	Sub	94	(T)₁₇=1.00	delTT=0.00, delT=0.00, dupT=0.00
Allele Frequency Aggregator	South Asian	Sub	86	(T)₁₇=1.00	delTT=0.00, delT=0.00, dupT=0.00
1000Genomes	Global	Study-wide	5008	(T)₁₇=0.8796	delT=0.1204
1000Genomes	African	Sub	1322	(T)₁₇=0.8396	delT=0.1604
1000Genomes	East Asian	Sub	1008	(T)₁₇=0.8770	delT=0.1230
1000Genomes	Europe	Sub	1006	(T)₁₇=0.8837	delT=0.1163
1000Genomes	South Asian	Sub	978	(T)₁₇=0.934	delT=0.066
1000Genomes	American	Sub	694	(T)₁₇=0.878	delT=0.122

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 5	NC_000005.10:g.149384922_149384926del
GRCh38.p14 chr 5	NC_000005.10:g.149384923_149384926del
GRCh38.p14 chr 5	NC_000005.10:g.149384924_149384926del
GRCh38.p14 chr 5	NC_000005.10:g.149384925_149384926del
GRCh38.p14 chr 5	NC_000005.10:g.149384926del
GRCh38.p14 chr 5	NC_000005.10:g.149384926dup
GRCh38.p14 chr 5	NC_000005.10:g.149384925_149384926dup
GRCh38.p14 chr 5	NC_000005.10:g.149384924_149384926dup
GRCh38.p14 chr 5	NC_000005.10:g.149384923_149384926dup
GRCh38.p14 chr 5	NC_000005.10:g.149384922_149384926dup
GRCh37.p13 chr 5	NC_000005.9:g.148764485_148764489del
GRCh37.p13 chr 5	NC_000005.9:g.148764486_148764489del
GRCh37.p13 chr 5	NC_000005.9:g.148764487_148764489del
GRCh37.p13 chr 5	NC_000005.9:g.148764488_148764489del
GRCh37.p13 chr 5	NC_000005.9:g.148764489del
GRCh37.p13 chr 5	NC_000005.9:g.148764489dup
GRCh37.p13 chr 5	NC_000005.9:g.148764488_148764489dup
GRCh37.p13 chr 5	NC_000005.9:g.148764487_148764489dup
GRCh37.p13 chr 5	NC_000005.9:g.148764486_148764489dup
GRCh37.p13 chr 5	NC_000005.9:g.148764485_148764489dup

Gene: IL17B, interleukin 17B (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
IL17B transcript variant 2	NM_001317987.2:c.-135-788… NM_001317987.2:c.-135-7889_-135-7885del	N/A	Intron Variant
IL17B transcript variant 1	NM_014443.3:c.	N/A	Genic Upstream Transcript Variant
IL17B transcript variant X2	XM_017009347.2:c.-135-788… XM_017009347.2:c.-135-7889_-135-7885del	N/A	Intron Variant
IL17B transcript variant X3	XM_017009348.2:c.-135-788… XM_017009348.2:c.-135-7889_-135-7885del	N/A	Intron Variant
IL17B transcript variant X1	XM_017009346.2:c.	N/A	Genic Upstream Transcript Variant
IL17B transcript variant X4	XM_047417104.1: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	(T)₁₇=	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅
GRCh38.p14 chr 5	NC_000005.10:g.149384910_149384926=	NC_000005.10:g.149384922_149384926del	NC_000005.10:g.149384923_149384926del	NC_000005.10:g.149384924_149384926del	NC_000005.10:g.149384925_149384926del	NC_000005.10:g.149384926del	NC_000005.10:g.149384926dup	NC_000005.10:g.149384925_149384926dup	NC_000005.10:g.149384924_149384926dup	NC_000005.10:g.149384923_149384926dup	NC_000005.10:g.149384922_149384926dup
GRCh37.p13 chr 5	NC_000005.9:g.148764473_148764489=	NC_000005.9:g.148764485_148764489del	NC_000005.9:g.148764486_148764489del	NC_000005.9:g.148764487_148764489del	NC_000005.9:g.148764488_148764489del	NC_000005.9:g.148764489del	NC_000005.9:g.148764489dup	NC_000005.9:g.148764488_148764489dup	NC_000005.9:g.148764487_148764489dup	NC_000005.9:g.148764486_148764489dup	NC_000005.9:g.148764485_148764489dup
IL17B transcript variant 2	NM_001317987.2:c.-135-7885=	NM_001317987.2:c.-135-7889_-135-7885del	NM_001317987.2:c.-135-7888_-135-7885del	NM_001317987.2:c.-135-7887_-135-7885del	NM_001317987.2:c.-135-7886_-135-7885del	NM_001317987.2:c.-135-7885del	NM_001317987.2:c.-135-7885dup	NM_001317987.2:c.-135-7886_-135-7885dup	NM_001317987.2:c.-135-7887_-135-7885dup	NM_001317987.2:c.-135-7888_-135-7885dup	NM_001317987.2:c.-135-7889_-135-7885dup
IL17B transcript variant X2	XM_017009347.2:c.-135-7885=	XM_017009347.2:c.-135-7889_-135-7885del	XM_017009347.2:c.-135-7888_-135-7885del	XM_017009347.2:c.-135-7887_-135-7885del	XM_017009347.2:c.-135-7886_-135-7885del	XM_017009347.2:c.-135-7885del	XM_017009347.2:c.-135-7885dup	XM_017009347.2:c.-135-7886_-135-7885dup	XM_017009347.2:c.-135-7887_-135-7885dup	XM_017009347.2:c.-135-7888_-135-7885dup	XM_017009347.2:c.-135-7889_-135-7885dup
IL17B transcript variant X3	XM_017009348.2:c.-135-7885=	XM_017009348.2:c.-135-7889_-135-7885del	XM_017009348.2:c.-135-7888_-135-7885del	XM_017009348.2:c.-135-7887_-135-7885del	XM_017009348.2:c.-135-7886_-135-7885del	XM_017009348.2:c.-135-7885del	XM_017009348.2:c.-135-7885dup	XM_017009348.2:c.-135-7886_-135-7885dup	XM_017009348.2:c.-135-7887_-135-7885dup	XM_017009348.2:c.-135-7888_-135-7885dup	XM_017009348.2:c.-135-7889_-135-7885dup

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#.

35 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SSIP	ss947156179	Aug 21, 2014 (142)
2	1000GENOMES	ss1374658046	Aug 21, 2014 (142)
3	SWEGEN	ss2997988386	Nov 08, 2017 (151)
4	PACBIO	ss3785281301	Jul 13, 2019 (153)
5	PACBIO	ss3790659151	Jul 13, 2019 (153)
6	PACBIO	ss3795536133	Jul 13, 2019 (153)
7	KHV_HUMAN_GENOMES	ss3807381110	Jul 13, 2019 (153)
8	EVA	ss3829563254	Apr 26, 2020 (154)
9	EVA	ss3838255634	Apr 26, 2020 (154)
10	EVA	ss3843698681	Apr 26, 2020 (154)
11	KOGIC	ss3957879168	Apr 26, 2020 (154)
12	KOGIC	ss3957879169	Apr 26, 2020 (154)
13	KOGIC	ss3957879170	Apr 26, 2020 (154)
14	GNOMAD	ss4131529776	Apr 26, 2021 (155)
15	GNOMAD	ss4131529777	Apr 26, 2021 (155)
16	GNOMAD	ss4131529778	Apr 26, 2021 (155)
17	GNOMAD	ss4131529779	Apr 26, 2021 (155)
18	GNOMAD	ss4131529780	Apr 26, 2021 (155)
19	GNOMAD	ss4131529781	Apr 26, 2021 (155)
20	GNOMAD	ss4131529782	Apr 26, 2021 (155)
21	GNOMAD	ss4131529783	Apr 26, 2021 (155)
22	GNOMAD	ss4131529784	Apr 26, 2021 (155)
23	GNOMAD	ss4131529785	Apr 26, 2021 (155)
24	TOMMO_GENOMICS	ss5174699150	Apr 26, 2021 (155)
25	TOMMO_GENOMICS	ss5174699151	Apr 26, 2021 (155)
26	TOMMO_GENOMICS	ss5174699152	Apr 26, 2021 (155)
27	1000G_HIGH_COVERAGE	ss5266273437	Oct 13, 2022 (156)
28	1000G_HIGH_COVERAGE	ss5266273438	Oct 13, 2022 (156)
29	1000G_HIGH_COVERAGE	ss5266273439	Oct 13, 2022 (156)
30	HUGCELL_USP	ss5464194055	Oct 13, 2022 (156)
31	HUGCELL_USP	ss5464194056	Oct 13, 2022 (156)
32	HUGCELL_USP	ss5464194057	Oct 13, 2022 (156)
33	TOMMO_GENOMICS	ss5711939725	Oct 13, 2022 (156)
34	TOMMO_GENOMICS	ss5711939726	Oct 13, 2022 (156)
35	TOMMO_GENOMICS	ss5711939727	Oct 13, 2022 (156)
36	1000Genomes	NC_000005.9 - 148764473	Oct 12, 2018 (152)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207992890 (NC_000005.10:149384909::T 553/121074) Row 207992891 (NC_000005.10:149384909::TT 6/121094) Row 207992892 (NC_000005.10:149384909::TTT 4/121108)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207992890 (NC_000005.10:149384909::T 553/121074) Row 207992891 (NC_000005.10:149384909::TT 6/121094) Row 207992892 (NC_000005.10:149384909::TTT 4/121108)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207992890 (NC_000005.10:149384909::T 553/121074) Row 207992891 (NC_000005.10:149384909::TT 6/121094) Row 207992892 (NC_000005.10:149384909::TTT 4/121108)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207992890 (NC_000005.10:149384909::T 553/121074) Row 207992891 (NC_000005.10:149384909::TT 6/121094) Row 207992892 (NC_000005.10:149384909::TTT 4/121108)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207992890 (NC_000005.10:149384909::T 553/121074) Row 207992891 (NC_000005.10:149384909::TT 6/121094) Row 207992892 (NC_000005.10:149384909::TTT 4/121108)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207992890 (NC_000005.10:149384909::T 553/121074) Row 207992891 (NC_000005.10:149384909::TT 6/121094) Row 207992892 (NC_000005.10:149384909::TTT 4/121108)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207992890 (NC_000005.10:149384909::T 553/121074) Row 207992891 (NC_000005.10:149384909::TT 6/121094) Row 207992892 (NC_000005.10:149384909::TTT 4/121108)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207992890 (NC_000005.10:149384909::T 553/121074) Row 207992891 (NC_000005.10:149384909::TT 6/121094) Row 207992892 (NC_000005.10:149384909::TTT 4/121108)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207992890 (NC_000005.10:149384909::T 553/121074) Row 207992891 (NC_000005.10:149384909::TT 6/121094) Row 207992892 (NC_000005.10:149384909::TTT 4/121108)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207992890 (NC_000005.10:149384909::T 553/121074) Row 207992891 (NC_000005.10:149384909::TT 6/121094) Row 207992892 (NC_000005.10:149384909::TTT 4/121108)...	-	Apr 26, 2021 (155)
47	Korean Genome Project Submission ignored due to conflicting rows: Row 14257169 (NC_000005.10:149384911::T 143/1830) Row 14257170 (NC_000005.10:149384910:T: 335/1830) Row 14257171 (NC_000005.10:149384909:TT: 13/1830)	-	Apr 26, 2020 (154)
48	Korean Genome Project Submission ignored due to conflicting rows: Row 14257169 (NC_000005.10:149384911::T 143/1830) Row 14257170 (NC_000005.10:149384910:T: 335/1830) Row 14257171 (NC_000005.10:149384909:TT: 13/1830)	-	Apr 26, 2020 (154)
49	Korean Genome Project Submission ignored due to conflicting rows: Row 14257169 (NC_000005.10:149384911::T 143/1830) Row 14257170 (NC_000005.10:149384910:T: 335/1830) Row 14257171 (NC_000005.10:149384909:TT: 13/1830)	-	Apr 26, 2020 (154)
50	8.3KJPN Submission ignored due to conflicting rows: Row 32668457 (NC_000005.9:148764472:T: 1031/16746) Row 32668458 (NC_000005.9:148764472::T 166/16746) Row 32668459 (NC_000005.9:148764472:TT: 3/16746)	-	Apr 26, 2021 (155)
51	8.3KJPN Submission ignored due to conflicting rows: Row 32668457 (NC_000005.9:148764472:T: 1031/16746) Row 32668458 (NC_000005.9:148764472::T 166/16746) Row 32668459 (NC_000005.9:148764472:TT: 3/16746)	-	Apr 26, 2021 (155)
52	8.3KJPN Submission ignored due to conflicting rows: Row 32668457 (NC_000005.9:148764472:T: 1031/16746) Row 32668458 (NC_000005.9:148764472::T 166/16746) Row 32668459 (NC_000005.9:148764472:TT: 3/16746)	-	Apr 26, 2021 (155)
53	14KJPN Submission ignored due to conflicting rows: Row 45776829 (NC_000005.10:149384909::T 303/28256) Row 45776830 (NC_000005.10:149384909:T: 1830/28256) Row 45776831 (NC_000005.10:149384909:TT: 8/28256)	-	Oct 13, 2022 (156)
54	14KJPN Submission ignored due to conflicting rows: Row 45776829 (NC_000005.10:149384909::T 303/28256) Row 45776830 (NC_000005.10:149384909:T: 1830/28256) Row 45776831 (NC_000005.10:149384909:TT: 8/28256)	-	Oct 13, 2022 (156)
55	14KJPN Submission ignored due to conflicting rows: Row 45776829 (NC_000005.10:149384909::T 303/28256) Row 45776830 (NC_000005.10:149384909:T: 1830/28256) Row 45776831 (NC_000005.10:149384909:TT: 8/28256)	-	Oct 13, 2022 (156)
56	ALFA	NC_000005.10 - 149384910	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
ss4131529785	NC_000005.10:149384909:TTTTT:	NC_000005.10:149384909:TTTTTTTTTTT… NC_000005.10:149384909:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4131529784	NC_000005.10:149384909:TTTT:	NC_000005.10:149384909:TTTTTTTTTTT… NC_000005.10:149384909:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4131529783	NC_000005.10:149384909:TTT:	NC_000005.10:149384909:TTTTTTTTTTT… NC_000005.10:149384909:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss5174699152	NC_000005.9:148764472:TT:	NC_000005.10:149384909:TTTTTTTTTTT… NC_000005.10:149384909:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3957879170, ss4131529782, ss5266273439, ss5464194057, ss5711939727	NC_000005.10:149384909:TT:	NC_000005.10:149384909:TTTTTTTTTTT… NC_000005.10:149384909:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
9316094369	NC_000005.10:149384909:TTTTTTTTTTT… NC_000005.10:149384909:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000005.10:149384909:TTTTTTTTTTT… NC_000005.10:149384909:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
29404742, ss1374658046, ss2997988386, ss3785281301, ss3790659151, ss3795536133, ss3838255634, ss5174699150	NC_000005.9:148764472:T:	NC_000005.10:149384909:TTTTTTTTTTT… NC_000005.10:149384909:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3807381110, ss3843698681, ss4131529781, ss5266273437, ss5464194055, ss5711939726	NC_000005.10:149384909:T:	NC_000005.10:149384909:TTTTTTTTTTT… NC_000005.10:149384909:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
9316094369	NC_000005.10:149384909:TTTTTTTTTTT… NC_000005.10:149384909:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000005.10:149384909:TTTTTTTTTTT… NC_000005.10:149384909:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3957879169	NC_000005.10:149384910:T:	NC_000005.10:149384909:TTTTTTTTTTT… NC_000005.10:149384909:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3829563254, ss5174699151	NC_000005.9:148764472::T	NC_000005.10:149384909:TTTTTTTTTTT… NC_000005.10:149384909:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss947156179	NC_000005.9:148764473::T	NC_000005.10:149384909:TTTTTTTTTTT… NC_000005.10:149384909:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4131529776, ss5266273438, ss5464194056, ss5711939725	NC_000005.10:149384909::T	NC_000005.10:149384909:TTTTTTTTTTT… NC_000005.10:149384909:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
9316094369	NC_000005.10:149384909:TTTTTTTTTTT… NC_000005.10:149384909:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000005.10:149384909:TTTTTTTTTTT… NC_000005.10:149384909:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3957879168	NC_000005.10:149384911::T	NC_000005.10:149384909:TTTTTTTTTTT… NC_000005.10:149384909:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4131529777	NC_000005.10:149384909::TT	NC_000005.10:149384909:TTTTTTTTTTT… NC_000005.10:149384909:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4131529778	NC_000005.10:149384909::TTT	NC_000005.10:149384909:TTTTTTTTTTT… NC_000005.10:149384909:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4131529779	NC_000005.10:149384909::TTTT	NC_000005.10:149384909:TTTTTTTTTTT… NC_000005.10:149384909:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4131529780	NC_000005.10:149384909::TTTTT	NC_000005.10:149384909:TTTTTTTTTTT… NC_000005.10:149384909:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(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 rs531690396

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

rs531690396