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rs863225429

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863225429(A;G)
Make rs863225429(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position49249543
GeneCCDC22
is asnp
is mentioned by
dbSNPrs863225429
ebirs863225429
HLIrs863225429
Exacrs863225429
Varsomers863225429
Maprs863225429
PheGenIrs863225429
hapmaprs863225429
1000 genomesrs863225429
hgdprs863225429
ensemblrs863225429
gopubmedrs863225429
geneviewrs863225429
scholarrs863225429
googlers863225429
pharmgkbrs863225429
gwascentralrs863225429
openSNPrs863225429
23andMers863225429
23andMe allrs863225429
SNP Nexus

SNPshotrs863225429
SNPdbers863225429
MSV3drs863225429
GWAS Ctlgrs863225429
Max Magnitude0
ClinVar
Risk rs863225429(G;G)
Alt rs863225429(G;G)
Reference rs863225429(A;A)
Significance Pathogenic
Disease Ritscher-schinzel syndrome 2
Variation info
Gene CCDC22
CLNDBN Ritscher-schinzel syndrome 2
Reversed 0
HGVS NC_000023.10:g.49106004A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000202351.1,