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rs587783112

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587783112(-;-)
Make rs587783112(-;C)
Make rs587783112(C;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position18595411
GeneCDKL5
is asnp
is mentioned by
dbSNPrs587783112
ebirs587783112
HLIrs587783112
Exacrs587783112
Varsomers587783112
Maprs587783112
PheGenIrs587783112
hapmaprs587783112
1000 genomesrs587783112
hgdprs587783112
ensemblrs587783112
gopubmedrs587783112
geneviewrs587783112
scholarrs587783112
googlers587783112
pharmgkbrs587783112
gwascentralrs587783112
openSNPrs587783112
23andMers587783112
23andMe allrs587783112
SNP Nexus

SNPshotrs587783112
SNPdbers587783112
MSV3drs587783112
GWAS Ctlgrs587783112
Max Magnitude0
ClinVar
Risk rs587783112(C;C)
Alt rs587783112(C;C)
Reference rs587783112(;)
Significance Pathogenic
Disease not provided
Variation info
Gene CDKL5
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.18613531dupC
CLNSRC
CLNACC RCV000144783.1,