Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y
Location

Chromosome 11:119185039 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs59003954

HGVS name

11:g.119185039C>T

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 22 transcripts and has 272 sample genotypes.

Variant displays