Original source

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

A/G | Ambiguity code: R | MAF: 0.42 (G)

Chromosome 12:52287653 (forward strand) | View in location tab


with COSMIC COSM147519 (A/G)

Most severe consequence
Evidence status

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

About this variant

This variant overlaps 5 transcripts and has 2511 individual genotypes.

Variation displays