Name: rs1491361782
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.

rs1491361782

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr9:8858829-8858831 (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: delTA
Variation Type: Indel Insertion and Deletion
Frequency: delTA=0.034125 (4284/125538, GnomAD)
delTA=0.00004 (1/28256, 14KJPN)
delTA=0.00006 (1/16748, 8.3KJPN) (+ 4 more)
delTA=0.00556 (66/11862, ALFA)
delTA=0.0776 (299/3854, ALSPAC)
delTA=0.0604 (224/3708, TWINSUK)
delTA=0.047 (28/600, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PTPRD : Intron Variant
PTPRD-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	HTRZ	HWEP
Total	Global	11862	ATA=0.99444	A=0.00556	0.988872	0.011128	0
European	Sub	7618	ATA=0.9940	A=0.0060	0.987923	0.012077	0
African	Sub	2816	ATA=0.9950	A=0.0050	0.990057	0.009943	0
African Others	Sub	108	ATA=1.000	A=0.000	1.0	0.0	N/A
African American	Sub	2708	ATA=0.9948	A=0.0052	0.98966	0.01034	0
Asian	Sub	108	ATA=1.000	A=0.000	1.0	0.0	N/A
East Asian	Sub	84	ATA=1.00	A=0.00	1.0	0.0	N/A
Other Asian	Sub	24	ATA=1.00	A=0.00	1.0	0.0	N/A
Latin American 1	Sub	146	ATA=0.993	A=0.007	0.986301	0.013699	0
Latin American 2	Sub	610	ATA=0.995	A=0.005	0.990164	0.009836	0
South Asian	Sub	94	ATA=1.00	A=0.00	1.0	0.0	N/A
Other	Sub	470	ATA=0.996	A=0.004	0.991489	0.008511	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
gnomAD - Genomes	Global	Study-wide	125538	ATA=0.965875	delTA=0.034125
gnomAD - Genomes	European	Sub	69722	ATA=0.95376	delTA=0.04624
gnomAD - Genomes	African	Sub	35866	ATA=0.98821	delTA=0.01179
gnomAD - Genomes	American	Sub	12254	ATA=0.96777	delTA=0.03223
gnomAD - Genomes	Ashkenazi Jewish	Sub	3010	ATA=0.9475	delTA=0.0525
gnomAD - Genomes	East Asian	Sub	2772	ATA=0.9975	delTA=0.0025
gnomAD - Genomes	Other	Sub	1914	ATA=0.9598	delTA=0.0402
14KJPN	JAPANESE	Study-wide	28256	ATA=0.99996	delTA=0.00004
8.3KJPN	JAPANESE	Study-wide	16748	ATA=0.99994	delTA=0.00006
Allele Frequency Aggregator	Total	Global	11862	ATA=0.99444	delTA=0.00556
Allele Frequency Aggregator	European	Sub	7618	ATA=0.9940	delTA=0.0060
Allele Frequency Aggregator	African	Sub	2816	ATA=0.9950	delTA=0.0050
Allele Frequency Aggregator	Latin American 2	Sub	610	ATA=0.995	delTA=0.005
Allele Frequency Aggregator	Other	Sub	470	ATA=0.996	delTA=0.004
Allele Frequency Aggregator	Latin American 1	Sub	146	ATA=0.993	delTA=0.007
Allele Frequency Aggregator	Asian	Sub	108	ATA=1.000	delTA=0.000
Allele Frequency Aggregator	South Asian	Sub	94	ATA=1.00	delTA=0.00
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	ATA=0.9224	delTA=0.0776
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	ATA=0.9396	delTA=0.0604
Northern Sweden	ACPOP	Study-wide	600	ATA=0.953	delTA=0.047

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 9	NC_000009.12:g.8858830_8858831del
GRCh37.p13 chr 9	NC_000009.11:g.8858830_8858831del
PTPRD RefSeqGene	NG_033963.1:g.1758894_1758895del

Gene: PTPRD, protein tyrosine phosphatase receptor type D (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PTPRD transcript variant 1	NM_002839.4:c.-103-124884… NM_002839.4:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant 5	NM_001040712.2:c.	N/A	Genic Upstream Transcript Variant
PTPRD transcript variant 6	NM_001171025.2:c.	N/A	Genic Upstream Transcript Variant
PTPRD transcript variant 7	NM_001377946.1:c.	N/A	Genic Upstream Transcript Variant
PTPRD transcript variant 8	NM_001377947.1:c.	N/A	Genic Upstream Transcript Variant
PTPRD transcript variant 9	NM_001377958.1:c.	N/A	Genic Upstream Transcript Variant
PTPRD transcript variant 10	NM_001378058.1:c.	N/A	Genic Upstream Transcript Variant
PTPRD transcript variant 2	NM_130391.4:c.	N/A	Genic Upstream Transcript Variant
PTPRD transcript variant 3	NM_130392.3:c.	N/A	Genic Upstream Transcript Variant
PTPRD transcript variant 4	NM_130393.3:c.	N/A	Genic Upstream Transcript Variant
PTPRD transcript variant X7	XM_006716817.5:c.-103-124… XM_006716817.5:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X24	XM_006716823.4:c.-103-124… XM_006716823.4:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X27	XM_006716825.5:c.-103-124… XM_006716825.5:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X40	XM_006716827.5:c.-103-124… XM_006716827.5:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X1	XM_017014958.3:c.-103-124… XM_017014958.3:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X2	XM_017014961.3:c.-103-124… XM_017014961.3:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X5	XM_017014963.3:c.-103-124… XM_017014963.3:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X4	XM_017014964.3:c.-103-124… XM_017014964.3:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X6	XM_017014965.3:c.-103-124… XM_017014965.3:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X8	XM_017014966.3:c.-103-124… XM_017014966.3:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X9	XM_017014967.3:c.-103-124… XM_017014967.3:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X10	XM_017014968.3:c.-103-124… XM_017014968.3:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X13	XM_017014969.3:c.-103-124… XM_017014969.3:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X12	XM_017014970.3:c.-103-124… XM_017014970.3:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X15	XM_017014971.3:c.-103-124… XM_017014971.3:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X16	XM_017014972.3:c.-103-124… XM_017014972.3:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X17	XM_017014974.3:c.-103-124… XM_017014974.3:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X20	XM_017014976.3:c.-103-124… XM_017014976.3:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X19	XM_017014977.3:c.-103-124… XM_017014977.3:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X22	XM_017014978.3:c.-103-124… XM_017014978.3:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X23	XM_017014979.3:c.-103-124… XM_017014979.3:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X33	XM_017014980.3:c.-103-124… XM_017014980.3:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X44	XM_017014982.3:c.-103-124… XM_017014982.3:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X45	XM_017014983.3:c.-103-124… XM_017014983.3:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X14	XM_024447625.2:c.-103-124… XM_024447625.2:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X3	XM_047423641.1:c.-103-124… XM_047423641.1:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X11	XM_047423642.1:c.-103-124… XM_047423642.1:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X21	XM_047423644.1:c.-103-124… XM_047423644.1:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X25	XM_047423645.1:c.-103-124… XM_047423645.1:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X28	XM_047423647.1:c.-103-124… XM_047423647.1:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X30	XM_047423649.1:c.-103-124… XM_047423649.1:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X31	XM_047423650.1:c.-103-124… XM_047423650.1:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X32	XM_047423651.1:c.-103-124… XM_047423651.1:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X34	XM_047423652.1:c.-103-124… XM_047423652.1:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X35	XM_047423653.1:c.-103-124… XM_047423653.1:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X36	XM_047423654.1:c.-103-124… XM_047423654.1:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X39	XM_047423657.1:c.-103-124… XM_047423657.1:c.-103-124884_-103-124883del	N/A	Intron Variant
PTPRD transcript variant X18	XM_047423643.1:c.	N/A	Genic Upstream Transcript Variant
PTPRD transcript variant X26	XM_047423646.1:c.	N/A	Genic Upstream Transcript Variant
PTPRD transcript variant X29	XM_047423648.1:c.	N/A	Genic Upstream Transcript Variant
PTPRD transcript variant X37	XM_047423655.1:c.	N/A	Genic Upstream Transcript Variant
PTPRD transcript variant X38	XM_047423656.1:c.	N/A	Genic Upstream Transcript Variant
PTPRD transcript variant X41	XM_047423658.1:c.	N/A	Genic Upstream Transcript Variant
PTPRD transcript variant X42	XM_047423659.1:c.	N/A	Genic Upstream Transcript Variant
PTPRD transcript variant X43	XM_047423660.1:c.	N/A	Genic Upstream Transcript Variant

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

Molecule type	Change	Amino acid[Codon]	SO Term
PTPRD-AS1 transcript variant 1	NR_121599.1:n.	N/A	Intron Variant
PTPRD-AS1 transcript variant 2	NR_121600.1: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	ATA=	delTA
GRCh38.p14 chr 9	NC_000009.12:g.8858829_8858831=	NC_000009.12:g.8858830_8858831del
GRCh37.p13 chr 9	NC_000009.11:g.8858829_8858831=	NC_000009.11:g.8858830_8858831del
PTPRD RefSeqGene	NG_033963.1:g.1758893_1758895=	NG_033963.1:g.1758894_1758895del
PTPRD transcript variant 1	NM_002839.3:c.-103-124883=	NM_002839.3:c.-103-124884_-103-124883del
PTPRD transcript variant 1	NM_002839.4:c.-103-124883=	NM_002839.4:c.-103-124884_-103-124883del
PTPRD transcript variant X1	XM_005251529.1:c.-103-124883=	XM_005251529.1:c.-103-124884_-103-124883del
PTPRD transcript variant X5	XM_005251533.1:c.-103-124883=	XM_005251533.1:c.-103-124884_-103-124883del
PTPRD transcript variant X7	XM_006716817.5:c.-103-124883=	XM_006716817.5:c.-103-124884_-103-124883del
PTPRD transcript variant X24	XM_006716823.4:c.-103-124883=	XM_006716823.4:c.-103-124884_-103-124883del
PTPRD transcript variant X27	XM_006716825.5:c.-103-124883=	XM_006716825.5:c.-103-124884_-103-124883del
PTPRD transcript variant X40	XM_006716827.5:c.-103-124883=	XM_006716827.5:c.-103-124884_-103-124883del
PTPRD transcript variant X1	XM_017014958.3:c.-103-124883=	XM_017014958.3:c.-103-124884_-103-124883del
PTPRD transcript variant X2	XM_017014961.3:c.-103-124883=	XM_017014961.3:c.-103-124884_-103-124883del
PTPRD transcript variant X5	XM_017014963.3:c.-103-124883=	XM_017014963.3:c.-103-124884_-103-124883del
PTPRD transcript variant X4	XM_017014964.3:c.-103-124883=	XM_017014964.3:c.-103-124884_-103-124883del
PTPRD transcript variant X6	XM_017014965.3:c.-103-124883=	XM_017014965.3:c.-103-124884_-103-124883del
PTPRD transcript variant X8	XM_017014966.3:c.-103-124883=	XM_017014966.3:c.-103-124884_-103-124883del
PTPRD transcript variant X9	XM_017014967.3:c.-103-124883=	XM_017014967.3:c.-103-124884_-103-124883del
PTPRD transcript variant X10	XM_017014968.3:c.-103-124883=	XM_017014968.3:c.-103-124884_-103-124883del
PTPRD transcript variant X13	XM_017014969.3:c.-103-124883=	XM_017014969.3:c.-103-124884_-103-124883del
PTPRD transcript variant X12	XM_017014970.3:c.-103-124883=	XM_017014970.3:c.-103-124884_-103-124883del
PTPRD transcript variant X15	XM_017014971.3:c.-103-124883=	XM_017014971.3:c.-103-124884_-103-124883del
PTPRD transcript variant X16	XM_017014972.3:c.-103-124883=	XM_017014972.3:c.-103-124884_-103-124883del
PTPRD transcript variant X17	XM_017014974.3:c.-103-124883=	XM_017014974.3:c.-103-124884_-103-124883del
PTPRD transcript variant X20	XM_017014976.3:c.-103-124883=	XM_017014976.3:c.-103-124884_-103-124883del
PTPRD transcript variant X19	XM_017014977.3:c.-103-124883=	XM_017014977.3:c.-103-124884_-103-124883del
PTPRD transcript variant X22	XM_017014978.3:c.-103-124883=	XM_017014978.3:c.-103-124884_-103-124883del
PTPRD transcript variant X23	XM_017014979.3:c.-103-124883=	XM_017014979.3:c.-103-124884_-103-124883del
PTPRD transcript variant X33	XM_017014980.3:c.-103-124883=	XM_017014980.3:c.-103-124884_-103-124883del
PTPRD transcript variant X44	XM_017014982.3:c.-103-124883=	XM_017014982.3:c.-103-124884_-103-124883del
PTPRD transcript variant X45	XM_017014983.3:c.-103-124883=	XM_017014983.3:c.-103-124884_-103-124883del
PTPRD transcript variant X14	XM_024447625.2:c.-103-124883=	XM_024447625.2:c.-103-124884_-103-124883del
PTPRD transcript variant X3	XM_047423641.1:c.-103-124883=	XM_047423641.1:c.-103-124884_-103-124883del
PTPRD transcript variant X11	XM_047423642.1:c.-103-124883=	XM_047423642.1:c.-103-124884_-103-124883del
PTPRD transcript variant X21	XM_047423644.1:c.-103-124883=	XM_047423644.1:c.-103-124884_-103-124883del
PTPRD transcript variant X25	XM_047423645.1:c.-103-124883=	XM_047423645.1:c.-103-124884_-103-124883del
PTPRD transcript variant X28	XM_047423647.1:c.-103-124883=	XM_047423647.1:c.-103-124884_-103-124883del
PTPRD transcript variant X30	XM_047423649.1:c.-103-124883=	XM_047423649.1:c.-103-124884_-103-124883del
PTPRD transcript variant X31	XM_047423650.1:c.-103-124883=	XM_047423650.1:c.-103-124884_-103-124883del
PTPRD transcript variant X32	XM_047423651.1:c.-103-124883=	XM_047423651.1:c.-103-124884_-103-124883del
PTPRD transcript variant X34	XM_047423652.1:c.-103-124883=	XM_047423652.1:c.-103-124884_-103-124883del
PTPRD transcript variant X35	XM_047423653.1:c.-103-124883=	XM_047423653.1:c.-103-124884_-103-124883del
PTPRD transcript variant X36	XM_047423654.1:c.-103-124883=	XM_047423654.1:c.-103-124884_-103-124883del
PTPRD transcript variant X39	XM_047423657.1:c.-103-124883=	XM_047423657.1:c.-103-124884_-103-124883del

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#.

12 SubSNP, 7 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EVA_UK10K_ALSPAC	ss1706319770	Jan 10, 2018 (151)
2	EVA_UK10K_TWINSUK	ss1706319881	Jan 10, 2018 (151)
3	JJLAB	ss2030950469	Jan 10, 2018 (151)
4	EVA_DECODE	ss3723436781	Jul 13, 2019 (153)
5	ACPOP	ss3736291776	Jul 13, 2019 (153)
6	EVA	ss3844739612	Apr 26, 2020 (154)
7	GNOMAD	ss4197215094	Apr 27, 2021 (155)
8	TOMMO_GENOMICS	ss5191993171	Apr 27, 2021 (155)
9	1000G_HIGH_COVERAGE	ss5279724107	Oct 18, 2022 (156)
10	HUGCELL_USP	ss5476014441	Oct 18, 2022 (156)
11	SANFORD_IMAGENETICS	ss5646864428	Oct 18, 2022 (156)
12	TOMMO_GENOMICS	ss5735018446	Oct 18, 2022 (156)
13	The Avon Longitudinal Study of Parents and Children	NC_000009.11 - 8858829	Oct 12, 2018 (152)
14	gnomAD - Genomes	NC_000009.12 - 8858829	Apr 27, 2021 (155)
15	Northern Sweden	NC_000009.11 - 8858829	Jul 13, 2019 (153)
16	8.3KJPN	NC_000009.11 - 8858829	Apr 27, 2021 (155)
17	14KJPN	NC_000009.12 - 8858829	Oct 18, 2022 (156)
18	UK 10K study - Twins	NC_000009.11 - 8858829	Oct 12, 2018 (152)
19	ALFA	NC_000009.12 - 8858829	Apr 27, 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
25063914, 9576641, 49962478, 25063914, ss1706319770, ss1706319881, ss2030950469, ss3736291776, ss5191993171, ss5646864428	NC_000009.11:8858828:AT:	NC_000009.12:8858828:ATA:A	(self)
317500142, 68855550, ss3723436781, ss3844739612, ss4197215094, ss5279724107, ss5476014441, ss5735018446	NC_000009.12:8858828:AT:	NC_000009.12:8858828:ATA:A	(self)
8217016493	NC_000009.12:8858828:ATA:A	NC_000009.12:8858828:ATA:A	(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 rs1491361782

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

rs1491361782