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: 0.49 (C)
Location

Chromosome 20:22032876 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs582426, rs57456154

HGVS name

20:g.22032876C>T

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

Variation displays