Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.16 (T)
Location

Chromosome 1:12203862 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs9430686, rs17881572

This variation has 3 HGVS names - click the plus to show

Variation displays