Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: 0.48 (T)
Location

Chromosome 4:73740307 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR051279

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

4:g.73740307A>T

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature, has 3317 sample genotypes and is mentioned in 75 citations.

Variant displays