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rs587783110

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783110(-;-)
Make rs587783110(-;A)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position18575494
GeneCDKL5
is asnp
is mentioned by
dbSNPrs587783110
ebirs587783110
HLIrs587783110
Exacrs587783110
Varsomers587783110
Maprs587783110
PheGenIrs587783110
hapmaprs587783110
1000 genomesrs587783110
hgdprs587783110
ensemblrs587783110
gopubmedrs587783110
geneviewrs587783110
scholarrs587783110
googlers587783110
pharmgkbrs587783110
gwascentralrs587783110
openSNPrs587783110
23andMers587783110
23andMe allrs587783110
SNP Nexus

SNPshotrs587783110
SNPdbers587783110
MSV3drs587783110
GWAS Ctlgrs587783110
Max Magnitude0
ClinVar
Risk rs587783110(;)
Alt rs587783110(;)
Reference rs587783110(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene CDKL5
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.18593614delA
CLNSRC
CLNACC RCV000144781.1,