Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.34 (T)

Chromosome 6:159907588 (forward strand) | View in location tab


with COSMIC COSM3761631 (C/T)

Most severe consequence
Evidence status


Archive dbSNP rs58693554, rs57966069

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

This variation has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, has 2515 individual genotypes and is mentioned in 2 citations.

Variation displays