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
 
Intergenic variant
HGVS name

19:g.13882487T>C

Variant displays