Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.46 (C)
Location

Chromosome 7:2538147 (forward strand) | View in location tab

Co-located

with COSMIC COSM452894 (T/C)

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 7 transcripts and has 3978 individual genotypes.

Variation displays