Original source

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

Alleles
A/C/G | Ancestral: G | Ambiguity code: V | MAF: 0.45 (A)
Location

Chromosome 15:74035775 (forward strand) | View in location tab

Co-located

with COSMIC COSM3754464 (A/G)

Most severe consequence
Evidence status

Synonyms

This variation has 36 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

Variation displays