Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.09 (G)
Location

Chromosome 10:99531546 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

10:g.99531546C>G

Genotyping chips

This variation has assays on: Illumina_ImmunoChip

Variation displays