Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.15 (G)
Location

Chromosome 12:48765827 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

12:g.48765827A>G

This variation has assays on 4 chips - click the plus to show

Variation displays