Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.46 (A)
Location

Chromosome 6:39324923 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs52821735, rs60887277

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