Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.04 (G)
Location

Chromosome 11:114058941 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

11:g.114058941C>G

About this variant

This variant overlaps 5 transcripts and has 2505 sample genotypes.

Variant displays