Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K|MAF: 0.01 (T)
Location

Chromosome 11:32387587 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and has 2591 sample genotypes.

Variant displays