Original source

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

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: 0.30 (C)
Location

Chromosome 8:22162781 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59217304, rs2234822

This variation has 9 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

Variation displays