Original source

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

Alleles
A/T|Ancestral: A|Ambiguity code: W|MAF: 0.29 (T)
Location

Chromosome 4:73743328 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR025956

Most severe consequence
 
3 prime UTR variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 3 transcripts, has 2553 sample genotypes and is mentioned in 8 citations.

Variant displays