Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.49 (G)
Location

Chromosome 7:151150662 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 3 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, HumanOmniExpress, Illumina_HumanOmni5

About this variant

This variant overlaps 2 transcripts and has 2841 individual genotypes.

Variation displays