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: 0.03 (G)
Location

Chromosome 20:9414186 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59409373, rs59372055

This variation has 10 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

Variation displays