Original source

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

Alleles
T/A/G | Ancestral: T | Ambiguity code: D | MAF: 0.02 (A)
Location

Chromosome 6:15523652 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 20 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays