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rs587783075

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783075(G;G)
Make rs587783075(G;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position18575492
GeneCDKL5
is asnp
is mentioned by
dbSNPrs587783075
ebirs587783075
HLIrs587783075
Exacrs587783075
Varsomers587783075
Maprs587783075
PheGenIrs587783075
hapmaprs587783075
1000 genomesrs587783075
hgdprs587783075
ensemblrs587783075
gopubmedrs587783075
geneviewrs587783075
scholarrs587783075
googlers587783075
pharmgkbrs587783075
gwascentralrs587783075
openSNPrs587783075
23andMers587783075
23andMe allrs587783075
SNP Nexus

SNPshotrs587783075
SNPdbers587783075
MSV3drs587783075
GWAS Ctlgrs587783075
Max Magnitude0
ClinVar
Risk rs587783075(G;G)
Alt rs587783075(G;G)
Reference rs587783075(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene CDKL5
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.18593612T>G
CLNSRC
CLNACC RCV000144737.1,