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 4:89726252 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 13 transcripts, has 2599 sample genotypes and is mentioned in 1 citation.

Variant displays