Original source

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

with HGMD-PUBLIC CR025956

Most severe consequence
 
3 prime UTR variant
Evidence status

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

This variant has assays on 5 chips - click the plus to show

About this variant

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

Variant displays