Original source

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

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

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

Co-located variant

HGMD-PUBLIC CR094129

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 2937 sample genotypes and is mentioned in 5 citations.

Variant displays