Original source

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

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

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


with HGMD-PUBLIC CR042175

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 4 HGVS names - 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 40 citations.

Variant displays