Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome 7:101125148 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

7:g.101125148G>A

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5

About this variant

This variant overlaps 1 transcript, has 1095 individual genotypes and is mentioned in 1 citation.

Variation displays