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rs786204960

From SNPedia

Orientationplus
Geno Mag Summary
(ATT;ATT) 0 common in clinvar
Make rs786204960(-;-)
Make rs786204960(-;ATT)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position18575422
GeneCDKL5
is asnp
is mentioned by
dbSNPrs786204960
ebirs786204960
HLIrs786204960
Exacrs786204960
Varsomers786204960
Maprs786204960
PheGenIrs786204960
hapmaprs786204960
1000 genomesrs786204960
hgdprs786204960
ensemblrs786204960
gopubmedrs786204960
geneviewrs786204960
scholarrs786204960
googlers786204960
pharmgkbrs786204960
gwascentralrs786204960
openSNPrs786204960
23andMers786204960
23andMe allrs786204960
SNP Nexus

SNPshotrs786204960
SNPdbers786204960
MSV3drs786204960
GWAS Ctlgrs786204960
Max Magnitude0
ClinVar
Risk rs786204960(;)
Alt rs786204960(;)
Reference rs786204960(ATT;ATT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CDKL5
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.18593542_18593544delATT
CLNSRC RettBASE (CDKL5)
CLNACC RCV000169982.1,