Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.17 (C)
Location

Chromosome 4:41259483 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3775258, rs58920615

This variation has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 14 transcripts and has 2826 individual genotypes.

Variation displays