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rs786204962

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204962(A;A)
Make rs786204962(A;G)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position18507155
GeneCDKL5
is asnp
is mentioned by
dbSNPrs786204962
ebirs786204962
HLIrs786204962
Exacrs786204962
Varsomers786204962
Maprs786204962
PheGenIrs786204962
hapmaprs786204962
1000 genomesrs786204962
hgdprs786204962
ensemblrs786204962
gopubmedrs786204962
geneviewrs786204962
scholarrs786204962
googlers786204962
pharmgkbrs786204962
gwascentralrs786204962
openSNPrs786204962
23andMers786204962
23andMe allrs786204962
SNP Nexus

SNPshotrs786204962
SNPdbers786204962
MSV3drs786204962
GWAS Ctlgrs786204962
Max Magnitude0
ClinVar
Risk rs786204962(A;A)
Alt rs786204962(A;A)
Reference rs786204962(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CDKL5
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.18525275G>A
CLNSRC RettBASE (CDKL5)
CLNACC RCV000169987.1,