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: 0.24 (T)
Location

Chromosome 22:35067186 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57663198, rs56600175

This variation has 3 HGVS names - click the plus to show

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

Variation displays