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: 0.46 (A)
Location

Chromosome 6:39357147 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs52821735, rs60887277

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

This variation has assays on 6 chips - click the plus to show

Variation displays