Original source

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

Alleles
C/G | Ancestral: A | Ambiguity code: S | MAF: 0.21 (C)
Location

Chromosome 22:24234734 (forward strand) | View in location tab

Co-located

with dbSNP rs56181615 (C/G)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs36224309

This variation has 2 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0

Variation displays