Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.01 (C)
Location

Chromosome 1:39897498 (forward strand)|View in location tab

Co-located variant

COSMIC COSM5021170

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs3170946

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 5 transcripts and has 2506 sample genotypes.

Variant displays