Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.44 (C)
Location

Chromosome 14:53944201 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57525489

HGVS name

14:g.53944201T>C

This variation has assays on 12 chips - click the plus to show

Variation displays