Original source

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

G/A | Ambiguity code: R

Chromosome 4:3511984 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs1730762, rs7442038

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 2 sample genotypes.

Variant displays