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rs587783149

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783149(C;C)
Make rs587783149(C;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position18598461
GeneCDKL5
is asnp
is mentioned by
dbSNPrs587783149
ebirs587783149
HLIrs587783149
Exacrs587783149
Varsomers587783149
Maprs587783149
PheGenIrs587783149
hapmaprs587783149
1000 genomesrs587783149
hgdprs587783149
ensemblrs587783149
gopubmedrs587783149
geneviewrs587783149
scholarrs587783149
googlers587783149
pharmgkbrs587783149
gwascentralrs587783149
openSNPrs587783149
23andMers587783149
23andMe allrs587783149
SNP Nexus

SNPshotrs587783149
SNPdbers587783149
MSV3drs587783149
GWAS Ctlgrs587783149
Max Magnitude0
ClinVar
Risk rs587783149(C;C)
Alt rs587783149(C;C)
Reference rs587783149(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CDKL5
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.18616581G>C
CLNSRC
CLNACC RCV000144825.1,