Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.34 (C)
Location

Chromosome 12:52322092 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

12:g.52322092T>C

This variant has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 1 transcript and has 3963 sample genotypes.

Variant displays