Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.49 (C)
Location

Chromosome 19:41820557 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

19:g.41820557T>C

Variation displays