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rs587783071

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783071(A;T)
Make rs587783071(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position18564498
GeneCDKL5
is asnp
is mentioned by
dbSNPrs587783071
ebirs587783071
HLIrs587783071
Exacrs587783071
Varsomers587783071
Maprs587783071
PheGenIrs587783071
hapmaprs587783071
1000 genomesrs587783071
hgdprs587783071
ensemblrs587783071
gopubmedrs587783071
geneviewrs587783071
scholarrs587783071
googlers587783071
pharmgkbrs587783071
gwascentralrs587783071
openSNPrs587783071
23andMers587783071
23andMe allrs587783071
SNP Nexus

SNPshotrs587783071
SNPdbers587783071
MSV3drs587783071
GWAS Ctlgrs587783071
Max Magnitude0
ClinVar
Risk rs587783071(T;T)
Alt rs587783071(T;T)
Reference rs587783071(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CDKL5
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.18582618A>T
CLNSRC
CLNACC RCV000144733.2,