Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.13 (C)
Location

Chromosome 20:45925376 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59009182

HGVS name

20:g.45925376T>C

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

Variation displays