Original source

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

G/A | Ancestral: A | Ambiguity code: R | MAF: 0.05 (A)

Chromosome 4:89726127 (forward strand) | View in location tab


with HGMD-PUBLIC CR094129

Most severe consequence
3 prime UTR variant
Evidence status

This variant has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts, has 2937 sample genotypes and is mentioned in 5 citations.

Variant displays