Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.20 (C)
Location

Chromosome 14:19919519 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

14:g.19919519T>C

Variation displays