Original source

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

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

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


with HGMD-PUBLIC CR025956

Most severe consequence
Evidence status

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

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

About this variant

This variant overlaps 3 transcripts, has 2553 individual genotypes and is mentioned in 7 citations.

Variation displays