Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.38 (A)

Chromosome 11:71435531 (forward strand) | View in location tab


with COSMIC COSM329305 (G/A)

Most severe consequence
Evidence status

Clinical significance


Archive dbSNP rs3184254

This variation has 8 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 8 transcripts and has 2512 individual genotypes.

Variation displays