Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.11 (T)

Chromosome 17:61483324 (forward strand) | View in location tab


with COSMIC COSM3755737 (C/T)

Most severe consequence
Evidence status


Archive dbSNP rs59840887

This variation has 4 HGVS names - click the plus to show

This variation has assays on 12 chips - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 2592 individual genotypes.

Variation displays