Original source

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

C/G | Ancestral: C | Ambiguity code: S | MAF: 0.08 (G)

Chromosome 1:186679065 (forward strand) | View in location tab


with COSMIC COSM146712 (C/G)

Most severe consequence
Evidence status


This variation has 5 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 6 transcripts, has 3781 individual genotypes and is mentioned in 25 citations.

Variation displays