Original source

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

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