Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.09 (G)
Location

Chromosome 12:8647970 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 9 HGVS names - click the plus to show

This variation has assays on 11 chips - click the plus to show

Variation displays