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dbSNP Short Genetic Variations

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

rs1453909134

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr6:138218233 (GRCh38.p14)
Alleles
T>C
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.000004 (1/249886, GnomAD_exome)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
PBOV1 : Missense Variant
ARFGEF3 : Intron Variant
Publications
0 citations
Genomic View
See rs on genome
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Genomic regions, transcripts, and products
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Software version is: 2.0.1.post820+afb47a3d