Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.10 (T)
Location

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

Co-located

with COSMIC COSM3755737 (C/T)

Most severe consequence
Evidence status

Synonyms

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 3999 individual genotypes.

Variation displays