Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.40 (C)
Location

Chromosome 22:19150744 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

22:g.19150744T>C

About this variant

This variant overlaps 1 transcript and has 2506 sample genotypes.

Variant displays