Original source

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

A/G | Ancestral: A | Ambiguity code: R | MAF: 0.02 (G)

Chromosome 3:142451002 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2505 sample genotypes.

Variant displays