Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.26 (T)
Location

Chromosome 4:73741338 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR042175

Most severe consequence
 
Intron variant
Evidence status

This variant has 4 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature, has 2874 sample genotypes and is mentioned in 39 citations.

Variant displays