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: 0.25 (G)

Chromosome 10:69382664 (forward strand) | View in location tab


with COSMIC COSM4144806 (G/A), COSM4144804 (G/A), COSM4144805 (G/A), COSM4144803 (G/A)

Most severe consequence
Evidence status


Archive dbSNP rs17850368, rs60876495

This variation has 8 HGVS names - click the plus to show

This variation has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts, has 2412 individual genotypes and is mentioned in 2 citations.

Variation displays