Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.38 (C)
Location

Chromosome 7:260547 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3196200, rs17149752

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2505 individual genotypes.

Variation displays