Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.05 (G)
Location

Chromosome 7:38977111 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

7:g.38977111A>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 1 transcript and has 2575 individual genotypes.

Variation displays