Original source

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

Alleles
T/G | Ambiguity code: K | MAF: 0.31 (T)
Location

Chromosome 6:160752914 (forward strand) | View in location tab

Co-located

with COSMIC COSM3829605 (T/G)

Most severe consequence
Evidence status

Synonyms

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

This variation has assays on 6 chips - click the plus to show

Variation displays