Original source

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

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

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