Original source

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

A/G | Ancestral: A | Ambiguity code: R | MAF: 0.45 (A)

Chromosome 4:119158004 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

Clinical significance

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 2 transcripts, has 3697 sample genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variant displays