Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.31 (A)
Location

Chromosome 22:29280706 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs5763127

This variation has 15 HGVS names - click the plus to show

Variation displays