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rs863225428

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863225428(A;G)
Make rs863225428(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position49235685
GeneCCDC22
is asnp
is mentioned by
dbSNPrs863225428
ebirs863225428
HLIrs863225428
Exacrs863225428
Varsomers863225428
Maprs863225428
PheGenIrs863225428
hapmaprs863225428
1000 genomesrs863225428
hgdprs863225428
ensemblrs863225428
gopubmedrs863225428
geneviewrs863225428
scholarrs863225428
googlers863225428
pharmgkbrs863225428
gwascentralrs863225428
openSNPrs863225428
23andMers863225428
23andMe allrs863225428
SNP Nexus

SNPshotrs863225428
SNPdbers863225428
MSV3drs863225428
GWAS Ctlgrs863225428
Max Magnitude0
ClinVar
Risk rs863225428(G;G)
Alt rs863225428(G;G)
Reference rs863225428(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.49092145A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000202354.1,