Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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