Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
 
Regulatory region variant
Evidence status

HGVS name

19:g.41820557T>C

About this variant

This variant overlaps 1 regulatory feature and has 2776 sample genotypes.

Variant displays