Name: rs143422113
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.

rs143422113

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:1029549-1029558 (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: delTT / delT / dupT / dupTT / dup(…
delTT / delT / dupT / dupTT / dup(T)₉
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.28837 (4833/16760, 8.3KJPN)
dupT=0.11361 (1190/10474, ALFA)
dupT=0.2881 (1845/6404, 1000G_30x) (+ 7 more)
dupT=0.2925 (1465/5008, 1000G)
dupT=0.2661 (1192/4480, Estonian)
dupT=0.2875 (1108/3854, ALSPAC)
dupT=0.2931 (1087/3708, TWINSUK)
dupT=0.3155 (578/1832, Korea1K)
dupT=0.298 (179/600, NorthernSweden)
dupT=0.40 (16/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: IDI2-AS1 : 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	10474	TTTTTTTTTT=0.88639	TTTTTTTT=0.00000, TTTTTTTTT=0.00000, TTTTTTTTTTT=0.11361, TTTTTTTTTTTT=0.00000	0.80485	0.032079	0.16307	32
European	Sub	8140	TTTTTTTTTT=0.8541	TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTT=0.1459, TTTTTTTTTTTT=0.0000	0.749386	0.041278	0.209337	32
African	Sub	1640	TTTTTTTTTT=1.0000	TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	70	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1570	TTTTTTTTTT=1.0000	TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	42	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	32	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	10	TTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	66	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	316	TTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	30	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	240	TTTTTTTTTT=0.992	TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.008, TTTTTTTTTTTT=0.000	0.983333	0.0	0.016667	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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
8.3KJPN	JAPANESE	Study-wide	16760	- No frequency provided	dupT=0.28837
Allele Frequency Aggregator	Total	Global	10474	(T)₁₀=0.88639	delTT=0.00000, delT=0.00000, dupT=0.11361, dupTT=0.00000
Allele Frequency Aggregator	European	Sub	8140	(T)₁₀=0.8541	delTT=0.0000, delT=0.0000, dupT=0.1459, dupTT=0.0000
Allele Frequency Aggregator	African	Sub	1640	(T)₁₀=1.0000	delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	316	(T)₁₀=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Other	Sub	240	(T)₁₀=0.992	delTT=0.000, delT=0.000, dupT=0.008, dupTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	66	(T)₁₀=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Asian	Sub	42	(T)₁₀=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	South Asian	Sub	30	(T)₁₀=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
1000Genomes_30x	Global	Study-wide	6404	- No frequency provided	dupT=0.2881
1000Genomes_30x	African	Sub	1786	- No frequency provided	dupT=0.2380
1000Genomes_30x	Europe	Sub	1266	- No frequency provided	dupT=0.2646
1000Genomes_30x	South Asian	Sub	1202	- No frequency provided	dupT=0.3802
1000Genomes_30x	East Asian	Sub	1170	- No frequency provided	dupT=0.3248
1000Genomes_30x	American	Sub	980	- No frequency provided	dupT=0.253
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupT=0.2925
1000Genomes	African	Sub	1322	- No frequency provided	dupT=0.2390
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupT=0.3214
1000Genomes	Europe	Sub	1006	- No frequency provided	dupT=0.2744
1000Genomes	South Asian	Sub	978	- No frequency provided	dupT=0.381
1000Genomes	American	Sub	694	- No frequency provided	dupT=0.254
Genetic variation in the Estonian population	Estonian	Study-wide	4480	- No frequency provided	dupT=0.2661
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	- No frequency provided	dupT=0.2875
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	- No frequency provided	dupT=0.2931
Korean Genome Project	KOREAN	Study-wide	1832	- No frequency provided	dupT=0.3155
Northern Sweden	ACPOP	Study-wide	600	- No frequency provided	dupT=0.298
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupT=0.40

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 10	NC_000010.11:g.1029557_1029558del
GRCh38.p14 chr 10	NC_000010.11:g.1029558del
GRCh38.p14 chr 10	NC_000010.11:g.1029558dup
GRCh38.p14 chr 10	NC_000010.11:g.1029557_1029558dup
GRCh38.p14 chr 10	NC_000010.11:g.1029550_1029558dup
GRCh37.p13 chr 10	NC_000010.10:g.1075497_1075498del
GRCh37.p13 chr 10	NC_000010.10:g.1075498del
GRCh37.p13 chr 10	NC_000010.10:g.1075498dup
GRCh37.p13 chr 10	NC_000010.10:g.1075497_1075498dup
GRCh37.p13 chr 10	NC_000010.10:g.1075490_1075498dup

Gene: IDI2-AS1, IDI2 antisense RNA 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
IDI2-AS1 transcript variant 1	NR_024628.1:n.	N/A	Intron Variant
IDI2-AS1 transcript variant 2	NR_024629.1:n.	N/A	Intron Variant
IDI2-AS1 transcript variant 3	NR_027708.1:n.	N/A	Intron Variant
IDI2-AS1 transcript variant 4	NR_027709.1: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)₁₀=	delTT	delT	dupT	dupTT	dup(T)₉
GRCh38.p14 chr 10	NC_000010.11:g.1029549_1029558=	NC_000010.11:g.1029557_1029558del	NC_000010.11:g.1029558del	NC_000010.11:g.1029558dup	NC_000010.11:g.1029557_1029558dup	NC_000010.11:g.1029550_1029558dup
GRCh37.p13 chr 10	NC_000010.10:g.1075489_1075498=	NC_000010.10:g.1075497_1075498del	NC_000010.10:g.1075498del	NC_000010.10:g.1075498dup	NC_000010.10:g.1075497_1075498dup	NC_000010.10:g.1075490_1075498dup

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#.

51 SubSNP, 16 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	GMI	ss287852888	Dec 06, 2013 (138)
2	GMI	ss288991276	May 04, 2012 (138)
3	1000GENOMES	ss327199768	May 09, 2011 (134)
4	1000GENOMES	ss327275293	May 09, 2011 (134)
5	1000GENOMES	ss499115048	May 04, 2012 (137)
6	LUNTER	ss551990833	Apr 25, 2013 (138)
7	LUNTER	ss552227744	Apr 25, 2013 (138)
8	LUNTER	ss553396551	Apr 25, 2013 (138)
9	SSMP	ss663949469	Apr 01, 2015 (144)
10	1000GENOMES	ss1368994441	Aug 21, 2014 (142)
11	EVA_GENOME_DK	ss1574134006	Apr 01, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1706604858	Apr 01, 2015 (144)
13	EVA_UK10K_TWINSUK	ss1706604948	Apr 01, 2015 (144)
14	HAMMER_LAB	ss1806215201	Sep 08, 2015 (146)
15	JJLAB	ss2030995573	Sep 14, 2016 (149)
16	SYSTEMSBIOZJU	ss2627434320	Nov 08, 2017 (151)
17	SWEGEN	ss3005797602	Nov 08, 2017 (151)
18	MCHAISSO	ss3063636827	Nov 08, 2017 (151)
19	BEROUKHIMLAB	ss3644290990	Oct 12, 2018 (152)
20	BIOINF_KMB_FNS_UNIBA	ss3645112499	Oct 12, 2018 (152)
21	EGCUT_WGS	ss3673327138	Jul 13, 2019 (153)
22	EVA_DECODE	ss3689112665	Jul 13, 2019 (153)
23	EVA_DECODE	ss3689112666	Jul 13, 2019 (153)
24	ACPOP	ss3736980692	Jul 13, 2019 (153)
25	PACBIO	ss3786555362	Jul 13, 2019 (153)
26	PACBIO	ss3791750225	Jul 13, 2019 (153)
27	PACBIO	ss3796631964	Jul 13, 2019 (153)
28	KHV_HUMAN_GENOMES	ss3813002511	Jul 13, 2019 (153)
29	EVA	ss3831920265	Apr 26, 2020 (154)
30	EVA	ss3839488649	Apr 26, 2020 (154)
31	EVA	ss3844954172	Apr 26, 2020 (154)
32	KOGIC	ss3967041487	Apr 26, 2020 (154)
33	GNOMAD	ss4211559214	Apr 26, 2021 (155)
34	GNOMAD	ss4211559215	Apr 26, 2021 (155)
35	GNOMAD	ss4211559216	Apr 26, 2021 (155)
36	GNOMAD	ss4211559217	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5195890102	Apr 26, 2021 (155)
38	1000G_HIGH_COVERAGE	ss5282626872	Oct 16, 2022 (156)
39	HUGCELL_USP	ss5478435340	Oct 16, 2022 (156)
40	EVA	ss5509876557	Oct 16, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5575883573	Oct 16, 2022 (156)
42	SANFORD_IMAGENETICS	ss5648505743	Oct 16, 2022 (156)
43	TOMMO_GENOMICS	ss5740629470	Oct 16, 2022 (156)
44	TOMMO_GENOMICS	ss5740629471	Oct 16, 2022 (156)
45	YY_MCH	ss5811117346	Oct 16, 2022 (156)
46	EVA	ss5823855205	Oct 16, 2022 (156)
47	EVA	ss5823855206	Oct 16, 2022 (156)
48	EVA	ss5823855207	Oct 16, 2022 (156)
49	EVA	ss5849397407	Oct 16, 2022 (156)
50	EVA	ss5877406056	Oct 16, 2022 (156)
51	EVA	ss5939785489	Oct 16, 2022 (156)
52	1000Genomes	NC_000010.10 - 1075489	Oct 12, 2018 (152)
53	1000Genomes_30x	NC_000010.11 - 1029549	Oct 16, 2022 (156)
54	The Avon Longitudinal Study of Parents and Children	NC_000010.10 - 1075489	Oct 12, 2018 (152)
55	Genetic variation in the Estonian population	NC_000010.10 - 1075489	Oct 12, 2018 (152)
56	The Danish reference pan genome	NC_000010.10 - 1075489	Apr 26, 2020 (154)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 341178687 (NC_000010.11:1029548::T 39579/138286) Row 341178688 (NC_000010.11:1029548::TT 2/138356) Row 341178689 (NC_000010.11:1029548:T: 3/138350)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 341178687 (NC_000010.11:1029548::T 39579/138286) Row 341178688 (NC_000010.11:1029548::TT 2/138356) Row 341178689 (NC_000010.11:1029548:T: 3/138350)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 341178687 (NC_000010.11:1029548::T 39579/138286) Row 341178688 (NC_000010.11:1029548::TT 2/138356) Row 341178689 (NC_000010.11:1029548:T: 3/138350)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 341178687 (NC_000010.11:1029548::T 39579/138286) Row 341178688 (NC_000010.11:1029548::TT 2/138356) Row 341178689 (NC_000010.11:1029548:T: 3/138350)...	-	Apr 26, 2021 (155)
61	Korean Genome Project	NC_000010.11 - 1029549	Apr 26, 2020 (154)
62	Northern Sweden	NC_000010.10 - 1075489	Jul 13, 2019 (153)
63	8.3KJPN	NC_000010.10 - 1075489	Apr 26, 2021 (155)
64	14KJPN Submission ignored due to conflicting rows: Row 74466574 (NC_000010.11:1029548::T 8193/28258) Row 74466575 (NC_000010.11:1029548::TT 1/28258)	-	Oct 16, 2022 (156)
65	14KJPN Submission ignored due to conflicting rows: Row 74466574 (NC_000010.11:1029548::T 8193/28258) Row 74466575 (NC_000010.11:1029548::TT 1/28258)	-	Oct 16, 2022 (156)
66	UK 10K study - Twins	NC_000010.10 - 1075489	Oct 12, 2018 (152)
67	ALFA	NC_000010.11 - 1029549	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)
rs143502137	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4211559217	NC_000010.11:1029548:TT:	NC_000010.11:1029548:TTTTTTTTTT:TT… NC_000010.11:1029548:TTTTTTTTTT:TTTTTTTT	(self)
4271994586	NC_000010.11:1029548:TTTTTTTTTT:TT… NC_000010.11:1029548:TTTTTTTTTT:TTTTTTTT	NC_000010.11:1029548:TTTTTTTTTT:TT… NC_000010.11:1029548:TTTTTTTTTT:TTTTTTTT	(self)
ss5509876557	NC_000010.10:1075488:T:	NC_000010.11:1029548:TTTTTTTTTT:TT… NC_000010.11:1029548:TTTTTTTTTT:TTTTTTTTT
ss3689112665, ss4211559216	NC_000010.11:1029548:T:	NC_000010.11:1029548:TTTTTTTTTT:TT… NC_000010.11:1029548:TTTTTTTTTT:TTTTTTTTT	(self)
4271994586	NC_000010.11:1029548:TTTTTTTTTT:TT… NC_000010.11:1029548:TTTTTTTTTT:TTTTTTTTT	NC_000010.11:1029548:TTTTTTTTTT:TT… NC_000010.11:1029548:TTTTTTTTTT:TTTTTTTTT	(self)
ss327199768, ss327275293, ss551990833, ss552227744, ss553396551	NC_000010.9:1065488::T	NC_000010.11:1029548:TTTTTTTTTT:TT… NC_000010.11:1029548:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss288991276	NC_000010.9:1065498::T	NC_000010.11:1029548:TTTTTTTTTT:TT… NC_000010.11:1029548:TTTTTTTTTT:TTTTTTTTTTT	(self)
48281749, 26824960, 19065386, 215838, 10265557, 53859409, 26824960, ss499115048, ss663949469, ss1368994441, ss1574134006, ss1706604858, ss1706604948, ss1806215201, ss2030995573, ss2627434320, ss3005797602, ss3644290990, ss3673327138, ss3736980692, ss3786555362, ss3791750225, ss3796631964, ss3831920265, ss3839488649, ss5195890102, ss5648505743, ss5823855205, ss5939785489	NC_000010.10:1075488::T	NC_000010.11:1029548:TTTTTTTTTT:TT… NC_000010.11:1029548:TTTTTTTTTT:TTTTTTTTTTT	(self)
63409508, 23419488, ss3063636827, ss3645112499, ss3813002511, ss3844954172, ss3967041487, ss4211559214, ss5282626872, ss5478435340, ss5575883573, ss5740629470, ss5811117346, ss5849397407, ss5877406056	NC_000010.11:1029548::T	NC_000010.11:1029548:TTTTTTTTTT:TT… NC_000010.11:1029548:TTTTTTTTTT:TTTTTTTTTTT	(self)
4271994586	NC_000010.11:1029548:TTTTTTTTTT:TT… NC_000010.11:1029548:TTTTTTTTTT:TTTTTTTTTTT	NC_000010.11:1029548:TTTTTTTTTT:TT… NC_000010.11:1029548:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss3689112666	NC_000010.11:1029549::T	NC_000010.11:1029548:TTTTTTTTTT:TT… NC_000010.11:1029548:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss287852888	NT_008705.16:1015498::T	NC_000010.11:1029548:TTTTTTTTTT:TT… NC_000010.11:1029548:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss5823855207	NC_000010.10:1075488::TT	NC_000010.11:1029548:TTTTTTTTTT:TT… NC_000010.11:1029548:TTTTTTTTTT:TTTTTTTTTTTT
ss4211559215, ss5740629471	NC_000010.11:1029548::TT	NC_000010.11:1029548:TTTTTTTTTT:TT… NC_000010.11:1029548:TTTTTTTTTT:TTTTTTTTTTTT	(self)
4271994586	NC_000010.11:1029548:TTTTTTTTTT:TT… NC_000010.11:1029548:TTTTTTTTTT:TTTTTTTTTTTT	NC_000010.11:1029548:TTTTTTTTTT:TT… NC_000010.11:1029548:TTTTTTTTTT:TTTTTTTTTTTT	(self)
ss5823855206	NC_000010.10:1075488::TTTTTTTTT	NC_000010.11:1029548:TTTTTTTTTT:TT… NC_000010.11:1029548:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTT

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2334703532	NC_000010.10:1075488:TT:	NC_000010.11:1029548:TTTTTTTTTT:TT… NC_000010.11:1029548:TTTTTTTTTT:TTTTTTTT

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs143422113

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

rs143422113