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dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

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.

rs1489190887

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr9:110941721 (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
C>G
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.000019 (5/264690, TOPMED)
G=0.000007 (1/140298, GnomAD)
G=0.00000 (0/14050, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
LPAR1 : Missense 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 14050 C=1.00000 G=0.00000 1.0 0.0 0.0 N/A
European Sub 9690 C=1.0000 G=0.0000 1.0 0.0 0.0 N/A
African Sub 2898 C=1.0000 G=0.0000 1.0 0.0 0.0 N/A
African Others Sub 114 C=1.000 G=0.000 1.0 0.0 0.0 N/A
African American Sub 2784 C=1.0000 G=0.0000 1.0 0.0 0.0 N/A
Asian Sub 112 C=1.000 G=0.000 1.0 0.0 0.0 N/A
East Asian Sub 86 C=1.00 G=0.00 1.0 0.0 0.0 N/A
Other Asian Sub 26 C=1.00 G=0.00 1.0 0.0 0.0 N/A
Latin American 1 Sub 146 C=1.000 G=0.000 1.0 0.0 0.0 N/A
Latin American 2 Sub 610 C=1.000 G=0.000 1.0 0.0 0.0 N/A
South Asian Sub 98 C=1.00 G=0.00 1.0 0.0 0.0 N/A
Other Sub 496 C=1.000 G=0.000 1.0 0.0 0.0 N/A


Help

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 C=0.999981 G=0.000019
gnomAD - Genomes Global Study-wide 140298 C=0.999993 G=0.000007
gnomAD - Genomes European Sub 75962 C=1.00000 G=0.00000
gnomAD - Genomes African Sub 42066 C=0.99998 G=0.00002
gnomAD - Genomes American Sub 13662 C=1.00000 G=0.00000
gnomAD - Genomes Ashkenazi Jewish Sub 3322 C=1.0000 G=0.0000
gnomAD - Genomes East Asian Sub 3134 C=1.0000 G=0.0000
gnomAD - Genomes Other Sub 2152 C=1.0000 G=0.0000
Allele Frequency Aggregator Total Global 14050 C=1.00000 G=0.00000
Allele Frequency Aggregator European Sub 9690 C=1.0000 G=0.0000
Allele Frequency Aggregator African Sub 2898 C=1.0000 G=0.0000
Allele Frequency Aggregator Latin American 2 Sub 610 C=1.000 G=0.000
Allele Frequency Aggregator Other Sub 496 C=1.000 G=0.000
Allele Frequency Aggregator Latin American 1 Sub 146 C=1.000 G=0.000
Allele Frequency Aggregator Asian Sub 112 C=1.000 G=0.000
Allele Frequency Aggregator South Asian Sub 98 C=1.00 G=0.00
Help

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.110941721C>G
GRCh37.p13 chr 9 NC_000009.11:g.113704001C>G
Gene: LPAR1, lysophosphatidic acid receptor 1 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
LPAR1 transcript variant 10 NM_001351404.2:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001338333.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 5 NM_001351399.2:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001338328.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 1 NM_001401.5:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001392.2:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 22 NM_001351416.2:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001338345.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 18 NM_001351412.2:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001338341.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 19 NM_001351413.2:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001338342.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 23 NM_001351417.2:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001338346.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 24 NM_001351418.2:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001338347.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 2 NM_057159.4:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_476500.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 13 NM_001351407.2:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001338336.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 12 NM_001351406.2:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001338335.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 20 NM_001351414.2:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001338343.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 21 NM_001351415.2:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001338344.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 8 NM_001351402.2:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001338331.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 4 NM_001351398.2:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001338327.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 11 NM_001351405.2:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001338334.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 17 NM_001351411.2:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001338340.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 14 NM_001351408.2:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001338337.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 16 NM_001351410.2:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001338339.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 6 NM_001351400.2:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001338329.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 15 NM_001351409.2:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001338338.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 3 NM_001351397.2:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001338326.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 7 NM_001351401.2:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001338330.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 9 NM_001351403.2:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001338332.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 25 NM_001351419.2:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001338348.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 26 NM_001351420.2:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001338349.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 52 NM_001387495.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374424.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 49 NM_001387492.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374421.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 39 NM_001387482.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374411.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 42 NM_001387485.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374414.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 60 NM_001387505.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374434.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 76 NM_001387521.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform c NP_001374450.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 48 NM_001387491.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374420.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 51 NM_001387494.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374423.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 72 NM_001387517.1:c.439G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform b NP_001374446.1:p.Val147Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 36 NM_001387479.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374408.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 62 NM_001387507.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374436.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 37 NM_001387480.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374409.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 29 NM_001387472.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374401.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 53 NM_001387496.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374425.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 57 NM_001387502.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374431.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 35 NM_001387478.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374407.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 40 NM_001387483.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374412.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 47 NM_001387490.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374419.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 71 NM_001387516.1:c.439G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform b NP_001374445.1:p.Val147Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 41 NM_001387484.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374413.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 38 NM_001387481.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374410.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 75 NM_001387520.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform c NP_001374449.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 70 NM_001387515.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374444.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 32 NM_001387475.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374404.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 44 NM_001387487.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374416.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 27 NM_001387470.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374399.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 58 NM_001387503.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374432.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 59 NM_001387504.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374433.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 64 NM_001387509.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374438.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 50 NM_001387493.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374422.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 56 NM_001387501.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374430.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 33 NM_001387476.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374405.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 74 NM_001387519.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform c NP_001374448.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 61 NM_001387506.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374435.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 68 NM_001387513.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374442.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 31 NM_001387474.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374403.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 63 NM_001387508.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374437.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 34 NM_001387477.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374406.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 66 NM_001387511.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374440.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 45 NM_001387488.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374417.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 43 NM_001387486.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374415.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 30 NM_001387473.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374402.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 28 NM_001387471.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374400.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 46 NM_001387489.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374418.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 73 NM_001387518.1:c.439G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform b NP_001374447.1:p.Val147Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 54 NM_001387497.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374426.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 55 NM_001387498.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374427.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 69 NM_001387514.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374443.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 65 NM_001387510.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374439.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant 67 NM_001387512.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform a NP_001374441.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
LPAR1 transcript variant X1 XM_047422903.1:c.493G>C V [GTG] > L [CTG] Coding Sequence Variant
lysophosphatidic acid receptor 1 isoform X1 XP_047278859.1:p.Val165Leu V (Val) > L (Leu) Missense Variant
Help

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
Help

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 C= G
GRCh38.p14 chr 9 NC_000009.12:g.110941721= NC_000009.12:g.110941721C>G
GRCh37.p13 chr 9 NC_000009.11:g.113704001= NC_000009.11:g.113704001C>G
LPAR1 transcript variant 1 NM_001401.5:c.493= NM_001401.5:c.493G>C
LPAR1 transcript variant 1 NM_001401.4:c.493= NM_001401.4:c.493G>C
LPAR1 transcript variant 1 NM_001401.3:c.493= NM_001401.3:c.493G>C
LPAR1 transcript variant 2 NM_057159.4:c.493= NM_057159.4:c.493G>C
LPAR1 transcript variant 2 NM_057159.3:c.493= NM_057159.3:c.493G>C
LPAR1 transcript variant 2 NM_057159.2:c.493= NM_057159.2:c.493G>C
LPAR1 transcript variant 16 NM_001351410.2:c.493= NM_001351410.2:c.493G>C
LPAR1 transcript variant 16 NM_001351410.1:c.493= NM_001351410.1:c.493G>C
LPAR1 transcript variant 15 NM_001351409.2:c.493= NM_001351409.2:c.493G>C
LPAR1 transcript variant 15 NM_001351409.1:c.493= NM_001351409.1:c.493G>C
LPAR1 transcript variant 13 NM_001351407.2:c.493= NM_001351407.2:c.493G>C
LPAR1 transcript variant 13 NM_001351407.1:c.493= NM_001351407.1:c.493G>C
LPAR1 transcript variant 19 NM_001351413.2:c.493= NM_001351413.2:c.493G>C
LPAR1 transcript variant 19 NM_001351413.1:c.493= NM_001351413.1:c.493G>C
LPAR1 transcript variant 18 NM_001351412.2:c.493= NM_001351412.2:c.493G>C
LPAR1 transcript variant 18 NM_001351412.1:c.493= NM_001351412.1:c.493G>C
LPAR1 transcript variant 14 NM_001351408.2:c.493= NM_001351408.2:c.493G>C
LPAR1 transcript variant 14 NM_001351408.1:c.493= NM_001351408.1:c.493G>C
LPAR1 transcript variant 21 NM_001351415.2:c.493= NM_001351415.2:c.493G>C
LPAR1 transcript variant 21 NM_001351415.1:c.493= NM_001351415.1:c.493G>C
LPAR1 transcript variant 24 NM_001351418.2:c.493= NM_001351418.2:c.493G>C
LPAR1 transcript variant 24 NM_001351418.1:c.493= NM_001351418.1:c.493G>C
LPAR1 transcript variant 20 NM_001351414.2:c.493= NM_001351414.2:c.493G>C
LPAR1 transcript variant 20 NM_001351414.1:c.493= NM_001351414.1:c.493G>C
LPAR1 transcript variant 22 NM_001351416.2:c.493= NM_001351416.2:c.493G>C
LPAR1 transcript variant 22 NM_001351416.1:c.493= NM_001351416.1:c.493G>C
LPAR1 transcript variant 17 NM_001351411.2:c.493= NM_001351411.2:c.493G>C
LPAR1 transcript variant 17 NM_001351411.1:c.493= NM_001351411.1:c.493G>C
LPAR1 transcript variant 23 NM_001351417.2:c.493= NM_001351417.2:c.493G>C
LPAR1 transcript variant 23 NM_001351417.1:c.493= NM_001351417.1:c.493G>C
LPAR1 transcript variant 4 NM_001351398.2:c.493= NM_001351398.2:c.493G>C
LPAR1 transcript variant 4 NM_001351398.1:c.493= NM_001351398.1:c.493G>C
LPAR1 transcript variant 7 NM_001351401.2:c.493= NM_001351401.2:c.493G>C
LPAR1 transcript variant 7 NM_001351401.1:c.493= NM_001351401.1:c.493G>C
LPAR1 transcript variant 12 NM_001351406.2:c.493= NM_001351406.2:c.493G>C
LPAR1 transcript variant 12 NM_001351406.1:c.493= NM_001351406.1:c.493G>C
LPAR1 transcript variant 6 NM_001351400.2:c.493= NM_001351400.2:c.493G>C
LPAR1 transcript variant 6 NM_001351400.1:c.493= NM_001351400.1:c.493G>C
LPAR1 transcript variant 26 NM_001351420.2:c.493= NM_001351420.2:c.493G>C
LPAR1 transcript variant 26 NM_001351420.1:c.493= NM_001351420.1:c.493G>C
LPAR1 transcript variant 5 NM_001351399.2:c.493= NM_001351399.2:c.493G>C
LPAR1 transcript variant 5 NM_001351399.1:c.493= NM_001351399.1:c.493G>C
LPAR1 transcript variant 8 NM_001351402.2:c.493= NM_001351402.2:c.493G>C
LPAR1 transcript variant 8 NM_001351402.1:c.493= NM_001351402.1:c.493G>C
LPAR1 transcript variant 25 NM_001351419.2:c.493= NM_001351419.2:c.493G>C
LPAR1 transcript variant 25 NM_001351419.1:c.493= NM_001351419.1:c.493G>C
LPAR1 transcript variant 11 NM_001351405.2:c.493= NM_001351405.2:c.493G>C
LPAR1 transcript variant 11 NM_001351405.1:c.493= NM_001351405.1:c.493G>C
LPAR1 transcript variant 10 NM_001351404.2:c.493= NM_001351404.2:c.493G>C
LPAR1 transcript variant 10 NM_001351404.1:c.493= NM_001351404.1:c.493G>C
LPAR1 transcript variant 3 NM_001351397.2:c.493= NM_001351397.2:c.493G>C
LPAR1 transcript variant 3 NM_001351397.1:c.493= NM_001351397.1:c.493G>C
LPAR1 transcript variant 9 NM_001351403.2:c.493= NM_001351403.2:c.493G>C
LPAR1 transcript variant 9 NM_001351403.1:c.493= NM_001351403.1:c.493G>C
LPAR1 transcript variant 51 NM_001387494.1:c.493= NM_001387494.1:c.493G>C
LPAR1 transcript variant 47 NM_001387490.1:c.493= NM_001387490.1:c.493G>C
LPAR1 transcript variant 49 NM_001387492.1:c.493= NM_001387492.1:c.493G>C
LPAR1 transcript variant 56 NM_001387501.1:c.493= NM_001387501.1:c.493G>C
LPAR1 transcript variant 55 NM_001387498.1:c.493= NM_001387498.1:c.493G>C
LPAR1 transcript variant 67 NM_001387512.1:c.493= NM_001387512.1:c.493G>C
LPAR1 transcript variant 68 NM_001387513.1:c.493= NM_001387513.1:c.493G>C
LPAR1 transcript variant 60 NM_001387505.1:c.493= NM_001387505.1:c.493G>C
LPAR1 transcript variant 46 NM_001387489.1:c.493= NM_001387489.1:c.493G>C
LPAR1 transcript variant 63 NM_001387508.1:c.493= NM_001387508.1:c.493G>C
LPAR1 transcript variant 52 NM_001387495.1:c.493= NM_001387495.1:c.493G>C
LPAR1 transcript variant 64 NM_001387509.1:c.493= NM_001387509.1:c.493G>C
LPAR1 transcript variant 72 NM_001387517.1:c.439= NM_001387517.1:c.439G>C
LPAR1 transcript variant 53 NM_001387496.1:c.493= NM_001387496.1:c.493G>C
LPAR1 transcript variant 41 NM_001387484.1:c.493= NM_001387484.1:c.493G>C
LPAR1 transcript variant 48 NM_001387491.1:c.493= NM_001387491.1:c.493G>C
LPAR1 transcript variant 62 NM_001387507.1:c.493= NM_001387507.1:c.493G>C
LPAR1 transcript variant 61 NM_001387506.1:c.493= NM_001387506.1:c.493G>C
LPAR1 transcript variant 30 NM_001387473.1:c.493= NM_001387473.1:c.493G>C
LPAR1 transcript variant X1 XM_047422903.1:c.493= XM_047422903.1:c.493G>C
LPAR1 transcript variant 66 NM_001387511.1:c.493= NM_001387511.1:c.493G>C
LPAR1 transcript variant 44 NM_001387487.1:c.493= NM_001387487.1:c.493G>C
LPAR1 transcript variant 36 NM_001387479.1:c.493= NM_001387479.1:c.493G>C
LPAR1 transcript variant 40 NM_001387483.1:c.493= NM_001387483.1:c.493G>C
LPAR1 transcript variant 31 NM_001387474.1:c.493= NM_001387474.1:c.493G>C
LPAR1 transcript variant 57 NM_001387502.1:c.493= NM_001387502.1:c.493G>C
LPAR1 transcript variant 65 NM_001387510.1:c.493= NM_001387510.1:c.493G>C
LPAR1 transcript variant 59 NM_001387504.1:c.493= NM_001387504.1:c.493G>C
LPAR1 transcript variant 35 NM_001387478.1:c.493= NM_001387478.1:c.493G>C
LPAR1 transcript variant 45 NM_001387488.1:c.493= NM_001387488.1:c.493G>C
LPAR1 transcript variant 50 NM_001387493.1:c.493= NM_001387493.1:c.493G>C
LPAR1 transcript variant 33 NM_001387476.1:c.493= NM_001387476.1:c.493G>C
LPAR1 transcript variant 34 NM_001387477.1:c.493= NM_001387477.1:c.493G>C
LPAR1 transcript variant 58 NM_001387503.1:c.493= NM_001387503.1:c.493G>C
LPAR1 transcript variant 54 NM_001387497.1:c.493= NM_001387497.1:c.493G>C
LPAR1 transcript variant 71 NM_001387516.1:c.439= NM_001387516.1:c.439G>C
LPAR1 transcript variant 37 NM_001387480.1:c.493= NM_001387480.1:c.493G>C
LPAR1 transcript variant 27 NM_001387470.1:c.493= NM_001387470.1:c.493G>C
LPAR1 transcript variant 29 NM_001387472.1:c.493= NM_001387472.1:c.493G>C
LPAR1 transcript variant 32 NM_001387475.1:c.493= NM_001387475.1:c.493G>C
LPAR1 transcript variant 43 NM_001387486.1:c.493= NM_001387486.1:c.493G>C
LPAR1 transcript variant 39 NM_001387482.1:c.493= NM_001387482.1:c.493G>C
LPAR1 transcript variant 38 NM_001387481.1:c.493= NM_001387481.1:c.493G>C
LPAR1 transcript variant 70 NM_001387515.1:c.493= NM_001387515.1:c.493G>C
LPAR1 transcript variant 73 NM_001387518.1:c.439= NM_001387518.1:c.439G>C
LPAR1 transcript variant 28 NM_001387471.1:c.493= NM_001387471.1:c.493G>C
LPAR1 transcript variant 42 NM_001387485.1:c.493= NM_001387485.1:c.493G>C
LPAR1 transcript variant 69 NM_001387514.1:c.493= NM_001387514.1:c.493G>C
LPAR1 transcript variant 76 NM_001387521.1:c.493= NM_001387521.1:c.493G>C
LPAR1 transcript variant 75 NM_001387520.1:c.493= NM_001387520.1:c.493G>C
LPAR1 transcript variant 74 NM_001387519.1:c.493= NM_001387519.1:c.493G>C
lysophosphatidic acid receptor 1 isoform a NP_001392.2:p.Val165= NP_001392.2:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_476500.1:p.Val165= NP_476500.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001338339.1:p.Val165= NP_001338339.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001338338.1:p.Val165= NP_001338338.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001338336.1:p.Val165= NP_001338336.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001338342.1:p.Val165= NP_001338342.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001338341.1:p.Val165= NP_001338341.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001338337.1:p.Val165= NP_001338337.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001338344.1:p.Val165= NP_001338344.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001338347.1:p.Val165= NP_001338347.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001338343.1:p.Val165= NP_001338343.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001338345.1:p.Val165= NP_001338345.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001338340.1:p.Val165= NP_001338340.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001338346.1:p.Val165= NP_001338346.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001338327.1:p.Val165= NP_001338327.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001338330.1:p.Val165= NP_001338330.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001338335.1:p.Val165= NP_001338335.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001338329.1:p.Val165= NP_001338329.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001338349.1:p.Val165= NP_001338349.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001338328.1:p.Val165= NP_001338328.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001338331.1:p.Val165= NP_001338331.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001338348.1:p.Val165= NP_001338348.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001338334.1:p.Val165= NP_001338334.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001338333.1:p.Val165= NP_001338333.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001338326.1:p.Val165= NP_001338326.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001338332.1:p.Val165= NP_001338332.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374423.1:p.Val165= NP_001374423.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374419.1:p.Val165= NP_001374419.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374421.1:p.Val165= NP_001374421.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374430.1:p.Val165= NP_001374430.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374427.1:p.Val165= NP_001374427.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374441.1:p.Val165= NP_001374441.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374442.1:p.Val165= NP_001374442.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374434.1:p.Val165= NP_001374434.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374418.1:p.Val165= NP_001374418.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374437.1:p.Val165= NP_001374437.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374424.1:p.Val165= NP_001374424.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374438.1:p.Val165= NP_001374438.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform b NP_001374446.1:p.Val147= NP_001374446.1:p.Val147Leu
lysophosphatidic acid receptor 1 isoform a NP_001374425.1:p.Val165= NP_001374425.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374413.1:p.Val165= NP_001374413.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374420.1:p.Val165= NP_001374420.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374436.1:p.Val165= NP_001374436.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374435.1:p.Val165= NP_001374435.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374402.1:p.Val165= NP_001374402.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform X1 XP_047278859.1:p.Val165= XP_047278859.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374440.1:p.Val165= NP_001374440.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374416.1:p.Val165= NP_001374416.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374408.1:p.Val165= NP_001374408.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374412.1:p.Val165= NP_001374412.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374403.1:p.Val165= NP_001374403.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374431.1:p.Val165= NP_001374431.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374439.1:p.Val165= NP_001374439.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374433.1:p.Val165= NP_001374433.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374407.1:p.Val165= NP_001374407.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374417.1:p.Val165= NP_001374417.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374422.1:p.Val165= NP_001374422.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374405.1:p.Val165= NP_001374405.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374406.1:p.Val165= NP_001374406.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374432.1:p.Val165= NP_001374432.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374426.1:p.Val165= NP_001374426.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform b NP_001374445.1:p.Val147= NP_001374445.1:p.Val147Leu
lysophosphatidic acid receptor 1 isoform a NP_001374409.1:p.Val165= NP_001374409.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374399.1:p.Val165= NP_001374399.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374401.1:p.Val165= NP_001374401.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374404.1:p.Val165= NP_001374404.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374415.1:p.Val165= NP_001374415.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374411.1:p.Val165= NP_001374411.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374410.1:p.Val165= NP_001374410.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374444.1:p.Val165= NP_001374444.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform b NP_001374447.1:p.Val147= NP_001374447.1:p.Val147Leu
lysophosphatidic acid receptor 1 isoform a NP_001374400.1:p.Val165= NP_001374400.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374414.1:p.Val165= NP_001374414.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform a NP_001374443.1:p.Val165= NP_001374443.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform c NP_001374450.1:p.Val165= NP_001374450.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform c NP_001374449.1:p.Val165= NP_001374449.1:p.Val165Leu
lysophosphatidic acid receptor 1 isoform c NP_001374448.1:p.Val165= NP_001374448.1:p.Val165Leu
Help

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, 3 Frequency submissions
No Submitter Submission ID Date (Build)
1 GNOMAD ss2748243497 Nov 08, 2017 (151)
2 GNOMAD ss2882208900 Nov 08, 2017 (151)
3 TOPMED ss4832534332 Apr 27, 2021 (155)
4 gnomAD - Genomes NC_000009.12 - 110941721 Apr 27, 2021 (155)
5 TopMed NC_000009.12 - 110941721 Apr 27, 2021 (155)
6 ALFA NC_000009.12 - 110941721 Apr 27, 2021 (155)
Help

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
ss2748243497, ss2882208900 NC_000009.11:113704000:C:G NC_000009.12:110941720:C:G (self)
335086402, 669911893, 3316716449, ss4832534332 NC_000009.12:110941720:C:G NC_000009.12:110941720:C:G (self)
Help

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

No publications for rs1489190887

Help

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.

Software version is: 2.0.1.post820+afb47a3d