Original source

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

C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.50 (T)

Chromosome 2:20889754 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs658947, rs3732142, rs60320904

This variation has 8 HGVS names - click the plus to show

This variation has assays on 9 chips - click the plus to show

Variation displays