Original source

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

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

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

Most severe consequence
Evidence status

Clinical significance

Synonyms

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

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 2 transcripts, has 3697 individual genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variation displays