Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.40 (C)
Location

Chromosome 19:49932605 (forward strand) | View in location tab

Co-located

with COSMIC COSM440013 (C/T)

Most severe consequence
Evidence status

This variation has 6 synonyms - click the plus to show

This variation has 10 HGVS names - click the plus to show

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

Variation displays