Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.33 (C)
Location

Chromosome 11:69821299 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

11:g.69821299T>C

About this variant

This variant overlaps 1 transcript and has 2511 sample genotypes.

Variant displays