Original source

Variants (including SNPs and indels) imported from dbSNP (release 136) | [View in dbSNP]

Alleles
T/C | Ancestral: C | Ambiguity code: Y
Location

Chromosome 19:13882487 (forward strand) | View in location tab

Most severe consequence
HGVS name

19:g.13882487T>C

Variation displays