Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.07 (A)
Location

Chromosome 4:94995637 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 2 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 3 transcripts and has 2772 individual genotypes.

Variation displays