Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.49 (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, has 1139 individual genotypes and is associated with 1 phenotype.

Variation displays