Name: rs1482007148
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.

rs1482007148

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:57153352-57153357 (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: delATA
Variation Type: Indel Insertion and Deletion
Frequency: delATA=0.000011 (3/264690, TOPMED)
delATA=0.000007 (1/140188, GnomAD)
delATA=0.00000 (0/14050, ALFA) (+ 1 more)
delATA=0.002 (1/600, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PSME3IP1 : 3 Prime UTR 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	HWEP
Total	Global	14050	ATAATA=1.00000	ATA=0.00000	1.0	N/A
European	Sub	9690	ATAATA=1.0000	ATA=0.0000	1.0	N/A
African	Sub	2898	ATAATA=1.0000	ATA=0.0000	1.0	N/A
African Others	Sub	114	ATAATA=1.000	ATA=0.000	1.0	N/A
African American	Sub	2784	ATAATA=1.0000	ATA=0.0000	1.0	N/A
Asian	Sub	112	ATAATA=1.000	ATA=0.000	1.0	N/A
East Asian	Sub	86	ATAATA=1.00	ATA=0.00	1.0	N/A
Other Asian	Sub	26	ATAATA=1.00	ATA=0.00	1.0	N/A
Latin American 1	Sub	146	ATAATA=1.000	ATA=0.000	1.0	N/A
Latin American 2	Sub	610	ATAATA=1.000	ATA=0.000	1.0	N/A
South Asian	Sub	98	ATAATA=1.00	ATA=0.00	1.0	N/A
Other	Sub	496	ATAATA=1.000	ATA=0.000	1.0	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
TopMed	Global	Study-wide	264690	(ATA)₂=0.999989	delATA=0.000011
gnomAD - Genomes	Global	Study-wide	140188	(ATA)₂=0.999993	delATA=0.000007
gnomAD - Genomes	European	Sub	75920	(ATA)₂=0.99999	delATA=0.00001
gnomAD - Genomes	African	Sub	42026	(ATA)₂=1.00000	delATA=0.00000
gnomAD - Genomes	American	Sub	13640	(ATA)₂=1.00000	delATA=0.00000
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	(ATA)₂=1.0000	delATA=0.0000
gnomAD - Genomes	East Asian	Sub	3128	(ATA)₂=1.0000	delATA=0.0000
gnomAD - Genomes	Other	Sub	2150	(ATA)₂=1.0000	delATA=0.0000
Allele Frequency Aggregator	Total	Global	14050	(ATA)₂=1.00000	delATA=0.00000
Allele Frequency Aggregator	European	Sub	9690	(ATA)₂=1.0000	delATA=0.0000
Allele Frequency Aggregator	African	Sub	2898	(ATA)₂=1.0000	delATA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	610	(ATA)₂=1.000	delATA=0.000
Allele Frequency Aggregator	Other	Sub	496	(ATA)₂=1.000	delATA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	(ATA)₂=1.000	delATA=0.000
Allele Frequency Aggregator	Asian	Sub	112	(ATA)₂=1.000	delATA=0.000
Allele Frequency Aggregator	South Asian	Sub	98	(ATA)₂=1.00	delATA=0.00
Northern Sweden	ACPOP	Study-wide	600	(ATA)₂=0.998	delATA=0.002

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 16	NC_000016.10:g.57153352ATA[1]
GRCh37.p13 chr 16	NC_000016.9:g.57187264ATA[1]

Gene: PSME3IP1, proteasome activator subunit 3 interacting protein 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PSME3IP1 transcript variant 3	NM_001354080.1:c.933_93… NM_001354080.1:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant 5	NM_001354082.1:c.933_93… NM_001354082.1:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant 2	NM_001354079.1:c.933_93… NM_001354079.1:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant 1	NM_001354078.1:c.933_93… NM_001354078.1:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant 10	NM_001354087.1:c.933_93… NM_001354087.1:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant 20	NM_024946.4:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant 8	NM_001354085.2:c.933_93… NM_001354085.2:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant 22	NM_001354098.2:c.933_93… NM_001354098.2:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant 13	NM_001354090.2:c.933_93… NM_001354090.2:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant 27	NM_001354103.2:c.933_93… NM_001354103.2:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant 17	NM_001354094.2:c.933_93… NM_001354094.2:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant 24	NM_001354100.2:c.933_93… NM_001354100.2:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant 19	NM_001354096.2:c.933_93… NM_001354096.2:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant 12	NM_001354089.2:c.933_93… NM_001354089.2:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant 4	NM_001354081.2:c.933_93… NM_001354081.2:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant 7	NM_001354084.2:c.933_93… NM_001354084.2:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant 9	NM_001354086.2:c.933_93… NM_001354086.2:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant 6	NM_001354083.2:c.933_93… NM_001354083.2:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant 26	NM_001354102.2:c.933_93… NM_001354102.2:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant 18	NM_001354095.2:c.933_93… NM_001354095.2:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant 25	NM_001354101.2:c.933_93… NM_001354101.2:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant 23	NM_001354099.2:c.933_93… NM_001354099.2:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant 15	NM_001354092.2:c.933_93… NM_001354092.2:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant 11	NM_001354088.2:c.933_93… NM_001354088.2:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant 14	NM_001354091.2:c.933_93… NM_001354091.2:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant 21	NM_001354097.2:c.933_93… NM_001354097.2:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant X17	XM_017023704.1:c.933_93… XM_017023704.1:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant X1	XM_047434668.1:c.933_93… XM_047434668.1:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant X2	XM_047434669.1:c.933_93… XM_047434669.1:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant X3	XM_047434670.1:c.933_93… XM_047434670.1:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant X4	XM_047434671.1:c.933_93… XM_047434671.1:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant X5	XM_047434672.1:c.933_93… XM_047434672.1:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant X6	XM_047434673.1:c.933_93… XM_047434673.1:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant X7	XM_047434675.1:c.933_93… XM_047434675.1:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant X8	XM_047434676.1:c.933_93… XM_047434676.1:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant X9	XM_017023681.3:c.933_93… XM_017023681.3:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant X10	XM_047434677.1:c.933_93… XM_047434677.1:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant X11	XM_047434678.1:c.933_93… XM_047434678.1:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant X12	XM_024450454.2:c.933_93… XM_024450454.2:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant X13	XM_047434679.1:c.933_93… XM_047434679.1:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant X14	XM_047434680.1:c.933_93… XM_047434680.1:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant X15	XM_047434681.1:c.933_93… XM_047434681.1:c.933_938=	N/A	3 Prime UTR Variant
PSME3IP1 transcript variant X16	XM_017023703.2:c.933_93… XM_017023703.2:c.933_938=	N/A	3 Prime UTR 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)₂=	delATA
GRCh38.p14 chr 16	NC_000016.10:g.57153352_57153357=	NC_000016.10:g.57153352ATA[1]
GRCh37.p13 chr 16	NC_000016.9:g.57187264_57187269=	NC_000016.9:g.57187264ATA[1]
PSME3IP1 transcript variant 20	NM_024946.4:c.933_938=	NM_024946.4:c.*933TAT[1]
FAM192A transcript variant 20	NM_024946.3:c.933_938=	NM_024946.3:c.*933TAT[1]
FAM192A transcript	NM_024946.2:c.933_938=	NM_024946.2:c.*933TAT[1]
PSME3IP1 transcript variant X9	XM_017023681.3:c.933_938=	XM_017023681.3:c.*933TAT[1]
PSME3IP1 transcript variant X3	XM_017023681.2:c.933_938=	XM_017023681.2:c.*933TAT[1]
FAM192A transcript variant X4	XM_017023681.1:c.933_938=	XM_017023681.1:c.*933TAT[1]
PSME3IP1 transcript variant 27	NM_001354103.2:c.933_938=	NM_001354103.2:c.*933TAT[1]
FAM192A transcript variant 27	NM_001354103.1:c.933_938=	NM_001354103.1:c.*933TAT[1]
PSME3IP1 transcript variant 26	NM_001354102.2:c.933_938=	NM_001354102.2:c.*933TAT[1]
FAM192A transcript variant 26	NM_001354102.1:c.933_938=	NM_001354102.1:c.*933TAT[1]
PSME3IP1 transcript variant 25	NM_001354101.2:c.933_938=	NM_001354101.2:c.*933TAT[1]
FAM192A transcript variant 25	NM_001354101.1:c.933_938=	NM_001354101.1:c.*933TAT[1]
PSME3IP1 transcript variant 23	NM_001354099.2:c.933_938=	NM_001354099.2:c.*933TAT[1]
FAM192A transcript variant 23	NM_001354099.1:c.933_938=	NM_001354099.1:c.*933TAT[1]
PSME3IP1 transcript variant 24	NM_001354100.2:c.933_938=	NM_001354100.2:c.*933TAT[1]
FAM192A transcript variant 24	NM_001354100.1:c.933_938=	NM_001354100.1:c.*933TAT[1]
PSME3IP1 transcript variant 22	NM_001354098.2:c.933_938=	NM_001354098.2:c.*933TAT[1]
FAM192A transcript variant 22	NM_001354098.1:c.933_938=	NM_001354098.1:c.*933TAT[1]
PSME3IP1 transcript variant 19	NM_001354096.2:c.933_938=	NM_001354096.2:c.*933TAT[1]
FAM192A transcript variant 19	NM_001354096.1:c.933_938=	NM_001354096.1:c.*933TAT[1]
PSME3IP1 transcript variant 15	NM_001354092.2:c.933_938=	NM_001354092.2:c.*933TAT[1]
FAM192A transcript variant 15	NM_001354092.1:c.933_938=	NM_001354092.1:c.*933TAT[1]
PSME3IP1 transcript variant 13	NM_001354090.2:c.933_938=	NM_001354090.2:c.*933TAT[1]
FAM192A transcript variant 13	NM_001354090.1:c.933_938=	NM_001354090.1:c.*933TAT[1]
PSME3IP1 transcript variant 8	NM_001354085.2:c.933_938=	NM_001354085.2:c.*933TAT[1]
FAM192A transcript variant 8	NM_001354085.1:c.933_938=	NM_001354085.1:c.*933TAT[1]
PSME3IP1 transcript variant 11	NM_001354088.2:c.933_938=	NM_001354088.2:c.*933TAT[1]
FAM192A transcript variant 11	NM_001354088.1:c.933_938=	NM_001354088.1:c.*933TAT[1]
PSME3IP1 transcript variant 7	NM_001354084.2:c.933_938=	NM_001354084.2:c.*933TAT[1]
FAM192A transcript variant 7	NM_001354084.1:c.933_938=	NM_001354084.1:c.*933TAT[1]
PSME3IP1 transcript variant 12	NM_001354089.2:c.933_938=	NM_001354089.2:c.*933TAT[1]
FAM192A transcript variant 12	NM_001354089.1:c.933_938=	NM_001354089.1:c.*933TAT[1]
PSME3IP1 transcript variant 14	NM_001354091.2:c.933_938=	NM_001354091.2:c.*933TAT[1]
FAM192A transcript variant 14	NM_001354091.1:c.933_938=	NM_001354091.1:c.*933TAT[1]
PSME3IP1 transcript variant 18	NM_001354095.2:c.933_938=	NM_001354095.2:c.*933TAT[1]
FAM192A transcript variant 18	NM_001354095.1:c.933_938=	NM_001354095.1:c.*933TAT[1]
PSME3IP1 transcript variant 17	NM_001354094.2:c.933_938=	NM_001354094.2:c.*933TAT[1]
FAM192A transcript variant 17	NM_001354094.1:c.933_938=	NM_001354094.1:c.*933TAT[1]
PSME3IP1 transcript variant 4	NM_001354081.2:c.933_938=	NM_001354081.2:c.*933TAT[1]
FAM192A transcript variant 4	NM_001354081.1:c.933_938=	NM_001354081.1:c.*933TAT[1]
PSME3IP1 transcript variant 21	NM_001354097.2:c.933_938=	NM_001354097.2:c.*933TAT[1]
FAM192A transcript variant 21	NM_001354097.1:c.933_938=	NM_001354097.1:c.*933TAT[1]
PSME3IP1 transcript variant 9	NM_001354086.2:c.933_938=	NM_001354086.2:c.*933TAT[1]
FAM192A transcript variant 9	NM_001354086.1:c.933_938=	NM_001354086.1:c.*933TAT[1]
PSME3IP1 transcript variant X12	XM_024450454.2:c.933_938=	XM_024450454.2:c.*933TAT[1]
PSME3IP1 transcript variant X9	XM_024450454.1:c.933_938=	XM_024450454.1:c.*933TAT[1]
PSME3IP1 transcript variant 6	NM_001354083.2:c.933_938=	NM_001354083.2:c.*933TAT[1]
FAM192A transcript variant 6	NM_001354083.1:c.933_938=	NM_001354083.1:c.*933TAT[1]
PSME3IP1 transcript variant X16	XM_017023703.2:c.933_938=	XM_017023703.2:c.*933TAT[1]
PSME3IP1 transcript variant X10	XM_017023703.1:c.933_938=	XM_017023703.1:c.*933TAT[1]
PSME3IP1 transcript variant X6	XM_047434673.1:c.933_938=	XM_047434673.1:c.*933TAT[1]
PSME3IP1 transcript variant X3	XM_047434670.1:c.933_938=	XM_047434670.1:c.*933TAT[1]
PSME3IP1 transcript variant X7	XM_047434675.1:c.933_938=	XM_047434675.1:c.*933TAT[1]
PSME3IP1 transcript variant X4	XM_047434671.1:c.933_938=	XM_047434671.1:c.*933TAT[1]
PSME3IP1 transcript variant X5	XM_047434672.1:c.933_938=	XM_047434672.1:c.*933TAT[1]
PSME3IP1 transcript variant X10	XM_047434677.1:c.933_938=	XM_047434677.1:c.*933TAT[1]
PSME3IP1 transcript variant X2	XM_047434669.1:c.933_938=	XM_047434669.1:c.*933TAT[1]
PSME3IP1 transcript variant 10	NM_001354087.1:c.933_938=	NM_001354087.1:c.*933TAT[1]
PSME3IP1 transcript variant 2	NM_001354079.1:c.933_938=	NM_001354079.1:c.*933TAT[1]
PSME3IP1 transcript variant 3	NM_001354080.1:c.933_938=	NM_001354080.1:c.*933TAT[1]
PSME3IP1 transcript variant X8	XM_047434676.1:c.933_938=	XM_047434676.1:c.*933TAT[1]
PSME3IP1 transcript variant X11	XM_047434678.1:c.933_938=	XM_047434678.1:c.*933TAT[1]
FAM192A transcript variant 16	NM_001354093.1:c.933_938=	NM_001354093.1:c.*933TAT[1]
PSME3IP1 transcript variant X13	XM_047434679.1:c.933_938=	XM_047434679.1:c.*933TAT[1]
PSME3IP1 transcript variant X14	XM_047434680.1:c.933_938=	XM_047434680.1:c.*933TAT[1]
PSME3IP1 transcript variant X15	XM_047434681.1:c.933_938=	XM_047434681.1:c.*933TAT[1]
PSME3IP1 transcript variant X1	XM_047434668.1:c.933_938=	XM_047434668.1:c.*933TAT[1]
PSME3IP1 transcript variant 5	NM_001354082.1:c.933_938=	NM_001354082.1:c.*933TAT[1]
PSME3IP1 transcript variant 1	NM_001354078.1:c.933_938=	NM_001354078.1:c.*933TAT[1]
PSME3IP1 transcript variant X17	XM_017023704.1:c.933_938=	XM_017023704.1:c.*933TAT[1]

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#.

3 SubSNP, 4 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ACPOP	ss3741543635	Jul 13, 2019 (153)
2	GNOMAD	ss4301630484	Apr 27, 2021 (155)
3	TOPMED	ss5016667744	Apr 27, 2021 (155)
4	gnomAD - Genomes	NC_000016.10 - 57153352	Apr 27, 2021 (155)
5	Northern Sweden	NC_000016.9 - 57187264	Jul 13, 2019 (153)
6	TopMed	NC_000016.10 - 57153352	Apr 27, 2021 (155)
7	ALFA	NC_000016.10 - 57153352	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
14828500, ss3741543635	NC_000016.9:57187263:ATA:	NC_000016.10:57153351:ATAATA:ATA	(self)
490638161, 232213405, ss4301630484, ss5016667744	NC_000016.10:57153351:ATA:	NC_000016.10:57153351:ATAATA:ATA	(self)
4161908918	NC_000016.10:57153351:ATAATA:ATA	NC_000016.10:57153351:ATAATA:ATA	(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 rs1482007148

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

rs1482007148