Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.43 (C)
Location

Chromosome 9:22125503 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

9:g.22125503G>C

This variation has assays on 6 chips - click the plus to show

Variation displays