Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 6:32580777 (forward strand) | View in location tab

Co-located

with COSMIC COSM4006425 (G/C)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17849964

This variation has 3 HGVS names - click the plus to show

Variation displays