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rs587783119

From SNPedia

Orientationplus
Geno Mag Summary
(AC;AC) 0 common in clinvar
Make rs587783119(-;-)
Make rs587783119(-;CA)
Make rs587783119(CA;CA)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position18609566
GeneCDKL5
is asnp
is mentioned by
dbSNPrs587783119
ebirs587783119
HLIrs587783119
Exacrs587783119
Varsomers587783119
Maprs587783119
PheGenIrs587783119
hapmaprs587783119
1000 genomesrs587783119
hgdprs587783119
ensemblrs587783119
gopubmedrs587783119
geneviewrs587783119
scholarrs587783119
googlers587783119
pharmgkbrs587783119
gwascentralrs587783119
openSNPrs587783119
23andMers587783119
23andMe allrs587783119
SNP Nexus

SNPshotrs587783119
SNPdbers587783119
MSV3drs587783119
GWAS Ctlgrs587783119
Max Magnitude0
ClinVar
Risk rs587783119(;)
Alt rs587783119(;)
Reference rs587783119(AC;AC)
Significance Pathogenic
Disease not provided
Variation info
Gene CDKL5
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.18627686_18627687delCA
CLNSRC
CLNACC RCV000144790.1,