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: 0.19 (C)
Location

Chromosome 22:31206201 (forward strand) | View in location tab

Co-located

with dbSNP rs56138957 (C/T)

Most severe consequence
Evidence status

Synonyms

This variation has 6 HGVS names - click the plus to show

Variation displays