Original source

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

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

Chromosome 9:22003718 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 36 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays