Name: rs58434982
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.

rs58434982

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:165934742-165934751 (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: delAAA / delAA / dupA / dupAA / du…
delAAA / delAA / dupA / dupAA / dupAAA
Variation Type: Indel Insertion and Deletion
Frequency: (A)₁₀=0.0254 (127/5008, 1000G)
(A)₁₀=0.0011 (5/4466, Estonian)
(A)₁₀=0.0011 (5/4452, ALFA) (+ 4 more)
(A)₁₀=0.0000 (0/3854, ALSPAC)
(A)₁₀=0.0000 (0/3708, TWINSUK)
(A)₁₀=0.002 (1/600, NorthernSweden)
(A)₁₀=0.03 (1/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TTC21B-AS1 : Non Coding Transcript Variant
TTC21B : 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	4452	AAAAAAAAAA=0.0011	AAAAAAA=0.0000, AAAAAAAA=0.0000, AAAAAAAAAAA=0.9989, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000	0.0	0.997754	0.002246	0
European	Sub	4444	AAAAAAAAAA=0.0011	AAAAAAA=0.0000, AAAAAAAA=0.0000, AAAAAAAAAAA=0.9989, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000	0.0	0.99775	0.00225	0
African	Sub	0	AAAAAAAAAA=0	AAAAAAA=0, AAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0	0	0	0	N/A
African Others	Sub	0	AAAAAAAAAA=0	AAAAAAA=0, AAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0	0	0	0	N/A
African American	Sub	0	AAAAAAAAAA=0	AAAAAAA=0, AAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0	0	0	0	N/A
Asian	Sub	0	AAAAAAAAAA=0	AAAAAAA=0, AAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0	0	0	0	N/A
East Asian	Sub	0	AAAAAAAAAA=0	AAAAAAA=0, AAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0	0	0	0	N/A
Other Asian	Sub	0	AAAAAAAAAA=0	AAAAAAA=0, AAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	0	AAAAAAAAAA=0	AAAAAAA=0, AAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 2	Sub	0	AAAAAAAAAA=0	AAAAAAA=0, AAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0	0	0	0	N/A
South Asian	Sub	0	AAAAAAAAAA=0	AAAAAAA=0, AAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0	0	0	0	N/A
Other	Sub	8	AAAAAAAAAA=0.0	AAAAAAA=0.0, AAAAAAAA=0.0, AAAAAAAAAAA=1.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0	0.0	1.0	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	- No frequency provided	dupA=0.9746
1000Genomes	African	Sub	1322	- No frequency provided	dupA=0.9675
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupA=0.9742
1000Genomes	Europe	Sub	1006	- No frequency provided	dupA=0.9781
1000Genomes	South Asian	Sub	978	- No frequency provided	dupA=0.978
1000Genomes	American	Sub	694	- No frequency provided	dupA=0.980
Genetic variation in the Estonian population	Estonian	Study-wide	4466	- No frequency provided	dupA=0.9989
Allele Frequency Aggregator	Total	Global	4452	(A)₁₀=0.0011	delAAA=0.0000, delAA=0.0000, dupA=0.9989, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	European	Sub	4444	(A)₁₀=0.0011	delAAA=0.0000, delAA=0.0000, dupA=0.9989, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	Other	Sub	8	(A)₁₀=0.0	delAAA=0.0, delAA=0.0, dupA=1.0, dupAA=0.0, dupAAA=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(A)₁₀=0	delAAA=0, delAA=0, dupA=0, dupAA=0, dupAAA=0
Allele Frequency Aggregator	Latin American 2	Sub	0	(A)₁₀=0	delAAA=0, delAA=0, dupA=0, dupAA=0, dupAAA=0
Allele Frequency Aggregator	South Asian	Sub	0	(A)₁₀=0	delAAA=0, delAA=0, dupA=0, dupAA=0, dupAAA=0
Allele Frequency Aggregator	African	Sub	0	(A)₁₀=0	delAAA=0, delAA=0, dupA=0, dupAA=0, dupAAA=0
Allele Frequency Aggregator	Asian	Sub	0	(A)₁₀=0	delAAA=0, delAA=0, dupA=0, dupAA=0, dupAAA=0
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	- No frequency provided	dupA=1.0000
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	- No frequency provided	dupA=1.0000
Northern Sweden	ACPOP	Study-wide	600	- No frequency provided	dupA=0.998
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupA=0.97

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.165934749_165934751del
GRCh38.p14 chr 2	NC_000002.12:g.165934750_165934751del
GRCh38.p14 chr 2	NC_000002.12:g.165934751dup
GRCh38.p14 chr 2	NC_000002.12:g.165934750_165934751dup
GRCh38.p14 chr 2	NC_000002.12:g.165934749_165934751dup
GRCh37.p13 chr 2	NC_000002.11:g.166791259_166791261del
GRCh37.p13 chr 2	NC_000002.11:g.166791260_166791261del
GRCh37.p13 chr 2	NC_000002.11:g.166791261dup
GRCh37.p13 chr 2	NC_000002.11:g.166791260_166791261dup
GRCh37.p13 chr 2	NC_000002.11:g.166791259_166791261dup
TTC21B RefSeqGene	NG_030345.1:g.24095_24097del
TTC21B RefSeqGene	NG_030345.1:g.24096_24097del
TTC21B RefSeqGene	NG_030345.1:g.24097dup
TTC21B RefSeqGene	NG_030345.1:g.24096_24097dup
TTC21B RefSeqGene	NG_030345.1:g.24095_24097dup

Gene: TTC21B, tetratricopeptide repeat domain 21B (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TTC21B transcript	NM_024753.5:c.711-1687_71… NM_024753.5:c.711-1687_711-1685del	N/A	Intron Variant
TTC21B transcript variant X4	XM_006712761.2:c.711-1687… XM_006712761.2:c.711-1687_711-1685del	N/A	Intron Variant
TTC21B transcript variant X3	XM_011511871.4:c.-40-1687… XM_011511871.4:c.-40-1687_-40-1685del	N/A	Intron Variant
TTC21B transcript variant X5	XM_011511872.3:c.711-1687… XM_011511872.3:c.711-1687_711-1685del	N/A	Intron Variant
TTC21B transcript variant X1	XM_017004967.2:c.711-1687… XM_017004967.2:c.711-1687_711-1685del	N/A	Intron Variant
TTC21B transcript variant X2	XM_047445870.1:c.-37-1285… XM_047445870.1:c.-37-1285_-37-1283del	N/A	Intron Variant

Gene: TTC21B-AS1, TTC21B antisense RNA 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TTC21B-AS1 transcript variant 1	NR_038983.1:n.236_238del	N/A	Non Coding Transcript Variant
TTC21B-AS1 transcript variant 1	NR_038983.1:n.237_238del	N/A	Non Coding Transcript Variant
TTC21B-AS1 transcript variant 1	NR_038983.1:n.238dup	N/A	Non Coding Transcript Variant
TTC21B-AS1 transcript variant 1	NR_038983.1:n.237_238dup	N/A	Non Coding Transcript Variant
TTC21B-AS1 transcript variant 1	NR_038983.1:n.236_238dup	N/A	Non Coding Transcript Variant
TTC21B-AS1 transcript variant 2	NR_038984.1: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	(A)₁₀=	delAAA	delAA	dupA	dupAA	dupAAA
GRCh38.p14 chr 2	NC_000002.12:g.165934742_165934751=	NC_000002.12:g.165934749_165934751del	NC_000002.12:g.165934750_165934751del	NC_000002.12:g.165934751dup	NC_000002.12:g.165934750_165934751dup	NC_000002.12:g.165934749_165934751dup
GRCh37.p13 chr 2	NC_000002.11:g.166791252_166791261=	NC_000002.11:g.166791259_166791261del	NC_000002.11:g.166791260_166791261del	NC_000002.11:g.166791261dup	NC_000002.11:g.166791260_166791261dup	NC_000002.11:g.166791259_166791261dup
TTC21B RefSeqGene	NG_030345.1:g.24088_24097=	NG_030345.1:g.24095_24097del	NG_030345.1:g.24096_24097del	NG_030345.1:g.24097dup	NG_030345.1:g.24096_24097dup	NG_030345.1:g.24095_24097dup
TTC21B-AS1 transcript variant 1	NR_038983.1:n.229_238=	NR_038983.1:n.236_238del	NR_038983.1:n.237_238del	NR_038983.1:n.238dup	NR_038983.1:n.237_238dup	NR_038983.1:n.236_238dup
TTC21B transcript	NM_024753.4:c.711-1685=	NM_024753.4:c.711-1687_711-1685del	NM_024753.4:c.711-1686_711-1685del	NM_024753.4:c.711-1685dup	NM_024753.4:c.711-1686_711-1685dup	NM_024753.4:c.711-1687_711-1685dup
TTC21B transcript	NM_024753.5:c.711-1685=	NM_024753.5:c.711-1687_711-1685del	NM_024753.5:c.711-1686_711-1685del	NM_024753.5:c.711-1685dup	NM_024753.5:c.711-1686_711-1685dup	NM_024753.5:c.711-1687_711-1685dup
TTC21B transcript variant X4	XM_006712761.2:c.711-1685=	XM_006712761.2:c.711-1687_711-1685del	XM_006712761.2:c.711-1686_711-1685del	XM_006712761.2:c.711-1685dup	XM_006712761.2:c.711-1686_711-1685dup	XM_006712761.2:c.711-1687_711-1685dup
TTC21B transcript variant X3	XM_011511871.4:c.-40-1685=	XM_011511871.4:c.-40-1687_-40-1685del	XM_011511871.4:c.-40-1686_-40-1685del	XM_011511871.4:c.-40-1685dup	XM_011511871.4:c.-40-1686_-40-1685dup	XM_011511871.4:c.-40-1687_-40-1685dup
TTC21B transcript variant X5	XM_011511872.3:c.711-1685=	XM_011511872.3:c.711-1687_711-1685del	XM_011511872.3:c.711-1686_711-1685del	XM_011511872.3:c.711-1685dup	XM_011511872.3:c.711-1686_711-1685dup	XM_011511872.3:c.711-1687_711-1685dup
TTC21B transcript variant X1	XM_017004967.2:c.711-1685=	XM_017004967.2:c.711-1687_711-1685del	XM_017004967.2:c.711-1686_711-1685del	XM_017004967.2:c.711-1685dup	XM_017004967.2:c.711-1686_711-1685dup	XM_017004967.2:c.711-1687_711-1685dup
TTC21B transcript variant X2	XM_047445870.1:c.-37-1283=	XM_047445870.1:c.-37-1285_-37-1283del	XM_047445870.1:c.-37-1284_-37-1283del	XM_047445870.1:c.-37-1283dup	XM_047445870.1:c.-37-1284_-37-1283dup	XM_047445870.1:c.-37-1285_-37-1283dup

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#.

57 SubSNP, 16 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss81117072	Dec 03, 2013 (138)
2	HGSV	ss81645682	Dec 04, 2013 (138)
3	HUMANGENOME_JCVI	ss95291699	Dec 05, 2013 (138)
4	BGI	ss104727264	Dec 06, 2013 (138)
5	GMI	ss154698862	Dec 01, 2009 (138)
6	BUSHMAN	ss193573595	Jul 04, 2010 (138)
7	BL	ss255962888	May 09, 2011 (138)
8	GMI	ss287709472	Dec 06, 2013 (138)
9	GMI	ss288248186	May 04, 2012 (138)
10	GMI	ss288248188	May 04, 2012 (137)
11	PJP	ss295012350	May 09, 2011 (137)
12	PJP	ss295012351	May 09, 2011 (137)
13	1000GENOMES	ss326272277	May 09, 2011 (138)
14	1000GENOMES	ss326288724	May 09, 2011 (138)
15	1000GENOMES	ss326374139	May 09, 2011 (138)
16	LUNTER	ss551144317	Apr 25, 2013 (138)
17	LUNTER	ss551207511	Apr 25, 2013 (138)
18	LUNTER	ss552949099	Apr 25, 2013 (138)
19	BILGI_BIOE	ss666173987	Apr 25, 2013 (138)
20	1000GENOMES	ss1369075405	Aug 21, 2014 (142)
21	DDI	ss1536315513	Apr 01, 2015 (144)
22	EVA_GENOME_DK	ss1575556827	Apr 01, 2015 (144)
23	EVA_UK10K_ALSPAC	ss1703266531	Apr 01, 2015 (144)
24	EVA_UK10K_TWINSUK	ss1703266665	Apr 01, 2015 (144)
25	HAMMER_LAB	ss1797855595	Sep 08, 2015 (146)
26	SYSTEMSBIOZJU	ss2624983978	Nov 08, 2017 (151)
27	SWEGEN	ss2990801565	Nov 08, 2017 (151)
28	BEROUKHIMLAB	ss3644106037	Oct 11, 2018 (152)
29	BIOINF_KMB_FNS_UNIBA	ss3645592740	Oct 11, 2018 (152)
30	URBANLAB	ss3647197155	Oct 11, 2018 (152)
31	EGCUT_WGS	ss3658669788	Jul 13, 2019 (153)
32	EVA_DECODE	ss3705346324	Jul 13, 2019 (153)
33	EVA_DECODE	ss3705346325	Jul 13, 2019 (153)
34	ACPOP	ss3729071493	Jul 13, 2019 (153)
35	PACBIO	ss3784055731	Jul 13, 2019 (153)
36	PACBIO	ss3789609337	Jul 13, 2019 (153)
37	PACBIO	ss3794482314	Jul 13, 2019 (153)
38	KHV_HUMAN_GENOMES	ss3802030332	Jul 13, 2019 (153)
39	EVA	ss3827333474	Apr 25, 2020 (154)
40	EVA	ss3837084238	Apr 25, 2020 (154)
41	EVA	ss3842503920	Apr 25, 2020 (154)
42	KOGIC	ss3949423341	Apr 25, 2020 (154)
43	KOGIC	ss3949423342	Apr 25, 2020 (154)
44	GNOMAD	ss4054952691	Apr 26, 2021 (155)
45	GNOMAD	ss4054952692	Apr 26, 2021 (155)
46	GNOMAD	ss4054952693	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5154941639	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5154941640	Apr 26, 2021 (155)
49	1000G_HIGH_COVERAGE	ss5250833101	Oct 12, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5250833102	Oct 12, 2022 (156)
51	HUGCELL_USP	ss5450565139	Oct 12, 2022 (156)
52	HUGCELL_USP	ss5450565140	Oct 12, 2022 (156)
53	TOMMO_GENOMICS	ss5685375025	Oct 12, 2022 (156)
54	TOMMO_GENOMICS	ss5685375026	Oct 12, 2022 (156)
55	EVA	ss5821123972	Oct 12, 2022 (156)
56	EVA	ss5852813657	Oct 12, 2022 (156)
57	EVA	ss5933324306	Oct 12, 2022 (156)
58	1000Genomes	NC_000002.11 - 166791252	Oct 11, 2018 (152)
59	The Avon Longitudinal Study of Parents and Children	NC_000002.11 - 166791252	Oct 11, 2018 (152)
60	Genetic variation in the Estonian population	NC_000002.11 - 166791252	Oct 11, 2018 (152)
61	The Danish reference pan genome	NC_000002.11 - 166791252	Apr 25, 2020 (154)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 80752149 (NC_000002.12:165934741::A 135027/137466) Row 80752150 (NC_000002.12:165934741::AA 1682/137452) Row 80752151 (NC_000002.12:165934741:AA: 3/137474)	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 80752149 (NC_000002.12:165934741::A 135027/137466) Row 80752150 (NC_000002.12:165934741::AA 1682/137452) Row 80752151 (NC_000002.12:165934741:AA: 3/137474)	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 80752149 (NC_000002.12:165934741::A 135027/137466) Row 80752150 (NC_000002.12:165934741::AA 1682/137452) Row 80752151 (NC_000002.12:165934741:AA: 3/137474)	-	Apr 26, 2021 (155)
65	Korean Genome Project Submission ignored due to conflicting rows: Row 5801342 (NC_000002.12:165934741::A 1727/1832) Row 5801343 (NC_000002.12:165934741::AA 88/1832)	-	Apr 25, 2020 (154)
66	Korean Genome Project Submission ignored due to conflicting rows: Row 5801342 (NC_000002.12:165934741::A 1727/1832) Row 5801343 (NC_000002.12:165934741::AA 88/1832)	-	Apr 25, 2020 (154)
67	Northern Sweden	NC_000002.11 - 166791252	Jul 13, 2019 (153)
68	8.3KJPN Submission ignored due to conflicting rows: Row 12910946 (NC_000002.11:166791251::A 15717/16758) Row 12910947 (NC_000002.11:166791251::AA 1031/16758)	-	Apr 26, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 12910946 (NC_000002.11:166791251::A 15717/16758) Row 12910947 (NC_000002.11:166791251::AA 1031/16758)	-	Apr 26, 2021 (155)
70	14KJPN Submission ignored due to conflicting rows: Row 19212129 (NC_000002.12:165934741::A 26495/28256) Row 19212130 (NC_000002.12:165934741::AA 1737/28256)	-	Oct 12, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 19212129 (NC_000002.12:165934741::A 26495/28256) Row 19212130 (NC_000002.12:165934741::AA 1737/28256)	-	Oct 12, 2022 (156)
72	UK 10K study - Twins	NC_000002.11 - 166791252	Oct 11, 2018 (152)
73	ALFA	NC_000002.12 - 165934742	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)
rs67706949	May 11, 2012 (137)
rs67706950	Feb 27, 2009 (130)
rs67706951	Feb 27, 2009 (130)
rs72064590	May 11, 2012 (137)
rs76428913	May 15, 2013 (138)
rs140105750	May 11, 2012 (137)
rs140491744	Sep 17, 2011 (135)
rs143924675	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
2910683190	NC_000002.12:165934741:AAAAAAAAAA:… NC_000002.12:165934741:AAAAAAAAAA:AAAAAAA	NC_000002.12:165934741:AAAAAAAAAA:… NC_000002.12:165934741:AAAAAAAAAA:AAAAAAA	(self)
ss4054952693	NC_000002.12:165934741:AA:	NC_000002.12:165934741:AAAAAAAAAA:… NC_000002.12:165934741:AAAAAAAAAA:AAAAAAAA	(self)
2910683190	NC_000002.12:165934741:AAAAAAAAAA:… NC_000002.12:165934741:AAAAAAAAAA:AAAAAAAA	NC_000002.12:165934741:AAAAAAAAAA:… NC_000002.12:165934741:AAAAAAAAAA:AAAAAAAA	(self)
ss255962888, ss288248186, ss326272277, ss326288724, ss326374139, ss551144317, ss551207511, ss552949099	NC_000002.10:166499497::A	NC_000002.12:165934741:AAAAAAAAAA:… NC_000002.12:165934741:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss295012350	NC_000002.10:166499501::A	NC_000002.12:165934741:AAAAAAAAAA:… NC_000002.12:165934741:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss295012351	NC_000002.10:166499504::A	NC_000002.12:165934741:AAAAAAAAAA:… NC_000002.12:165934741:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss288248188	NC_000002.10:166499507::A	NC_000002.12:165934741:AAAAAAAAAA:… NC_000002.12:165934741:AAAAAAAAAA:AAAAAAAAAAA	(self)
11324766, 6247903, 4408036, 710723, 2356358, 6247903, ss666173987, ss1369075405, ss1536315513, ss1575556827, ss1703266531, ss1703266665, ss1797855595, ss2624983978, ss2990801565, ss3644106037, ss3658669788, ss3729071493, ss3784055731, ss3789609337, ss3794482314, ss3827333474, ss3837084238, ss5154941639, ss5821123972	NC_000002.11:166791251::A	NC_000002.12:165934741:AAAAAAAAAA:… NC_000002.12:165934741:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss3645592740, ss3647197155, ss3705346325, ss3802030332, ss3842503920, ss3949423341, ss4054952691, ss5250833101, ss5450565139, ss5685375025, ss5852813657, ss5933324306	NC_000002.12:165934741::A	NC_000002.12:165934741:AAAAAAAAAA:… NC_000002.12:165934741:AAAAAAAAAA:AAAAAAAAAAA	(self)
2910683190	NC_000002.12:165934741:AAAAAAAAAA:… NC_000002.12:165934741:AAAAAAAAAA:AAAAAAAAAAA	NC_000002.12:165934741:AAAAAAAAAA:… NC_000002.12:165934741:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss154698862	NT_005403.17:17000669::A	NC_000002.12:165934741:AAAAAAAAAA:… NC_000002.12:165934741:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss104727264	NT_005403.17:17000678::A	NC_000002.12:165934741:AAAAAAAAAA:… NC_000002.12:165934741:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss81117072, ss81645682, ss95291699, ss287709472	NT_005403.17:17000679::A	NC_000002.12:165934741:AAAAAAAAAA:… NC_000002.12:165934741:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss193573595	NT_005403.18:71438726::A	NC_000002.12:165934741:AAAAAAAAAA:… NC_000002.12:165934741:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss5154941640	NC_000002.11:166791251::AA	NC_000002.12:165934741:AAAAAAAAAA:… NC_000002.12:165934741:AAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3705346324, ss3949423342, ss4054952692, ss5250833102, ss5450565140, ss5685375026	NC_000002.12:165934741::AA	NC_000002.12:165934741:AAAAAAAAAA:… NC_000002.12:165934741:AAAAAAAAAA:AAAAAAAAAAAA	(self)
2910683190	NC_000002.12:165934741:AAAAAAAAAA:… NC_000002.12:165934741:AAAAAAAAAA:AAAAAAAAAAAA	NC_000002.12:165934741:AAAAAAAAAA:… NC_000002.12:165934741:AAAAAAAAAA:AAAAAAAAAAAA	(self)
2910683190	NC_000002.12:165934741:AAAAAAAAAA:… NC_000002.12:165934741:AAAAAAAAAA:AAAAAAAAAAAAA	NC_000002.12:165934741:AAAAAAAAAA:… NC_000002.12:165934741: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 rs58434982

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

rs58434982