Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.18 (G)
Location

Chromosome 12:48502100 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60037666

This variation has 12 HGVS names - click the plus to show

This variation has assays on 7 chips - click the plus to show

Variation displays