Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.38 (G)

Chromosome 11:47444403 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 5 transcripts, has 2776 sample genotypes and is associated with 2 phenotypes.

Variant displays