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rs587783081

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783081(C;T)
Make rs587783081(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position18581900
GeneCDKL5
is asnp
is mentioned by
dbSNPrs587783081
ebirs587783081
HLIrs587783081
Exacrs587783081
Varsomers587783081
Maprs587783081
PheGenIrs587783081
hapmaprs587783081
1000 genomesrs587783081
hgdprs587783081
ensemblrs587783081
gopubmedrs587783081
geneviewrs587783081
scholarrs587783081
googlers587783081
pharmgkbrs587783081
gwascentralrs587783081
openSNPrs587783081
23andMers587783081
23andMe allrs587783081
SNP Nexus

SNPshotrs587783081
SNPdbers587783081
MSV3drs587783081
GWAS Ctlgrs587783081
Max Magnitude0
ClinVar
Risk rs587783081(T;T)
Alt rs587783081(T;T)
Reference rs587783081(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CDKL5
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.18600020C>T
CLNSRC
CLNACC RCV000144743.2,