Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.01 (C)
Location

Chromosome 11:119185059 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

11:g.119185059G>C

About this variant

This variant overlaps 22 transcripts and has 2504 sample genotypes.

Variant displays