Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ambiguity code: R
Location

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

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs1730762, rs7442038

This variant has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2 sample genotypes.

Variant displays