Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)

Chromosome 3:46858235 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status

Clinical significance

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts, has 2504 sample genotypes and is associated with 1 phenotype.

Variant displays