Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: < 0.01 (G)
Location

Chromosome 2:9723813 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

2:g.9723813T>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays