Original source

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

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: 0.11 (T)
Location

Chromosome 6:98835500 (forward strand) | View in location tab

Co-located

with COSMIC COSM3749991 (T/G)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17846480, rs17859539

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript and has 2505 individual genotypes.

Variation displays