Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.41 (T)
Location

Chromosome 12:21840338 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17698626, rs60706895

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

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

Variation displays