Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.02 (G)
Location

Chromosome 5:159315876 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 5 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 4 transcripts, has 2533 individual genotypes and is mentioned in 3 citations.

Variation displays