Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.49 (G)
Location

Chromosome 12:20846411 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57087746

This variation has 6 HGVS names - click the plus to show

This variation has assays on 10 chips - click the plus to show

Variation displays