Original source

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

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

Chromosome 20:21872462 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58361976

HGVS name

20:g.21872462C>T

This variation has assays on 13 chips - click the plus to show

Variation displays