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rs863225065

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225065(C;T)
Make rs863225065(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position18604821
GeneCDKL5
is asnp
is mentioned by
dbSNPrs863225065
ebirs863225065
HLIrs863225065
Exacrs863225065
Varsomers863225065
Maprs863225065
PheGenIrs863225065
hapmaprs863225065
1000 genomesrs863225065
hgdprs863225065
ensemblrs863225065
gopubmedrs863225065
geneviewrs863225065
scholarrs863225065
googlers863225065
pharmgkbrs863225065
gwascentralrs863225065
openSNPrs863225065
23andMers863225065
23andMe allrs863225065
SNP Nexus

SNPshotrs863225065
SNPdbers863225065
MSV3drs863225065
GWAS Ctlgrs863225065
Max Magnitude0
ClinVar
Risk rs863225065(T;T)
Alt rs863225065(T;T)
Reference rs863225065(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CDKL5
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.18622941C>T
CLNSRC
CLNACC RCV000201269.1,