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rs786204967

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs786204967(-;-)
Make rs786204967(-;AG)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position18604171
GeneCDKL5
is asnp
is mentioned by
dbSNPrs786204967
ebirs786204967
HLIrs786204967
Exacrs786204967
Varsomers786204967
Maprs786204967
PheGenIrs786204967
hapmaprs786204967
1000 genomesrs786204967
hgdprs786204967
ensemblrs786204967
gopubmedrs786204967
geneviewrs786204967
scholarrs786204967
googlers786204967
pharmgkbrs786204967
gwascentralrs786204967
openSNPrs786204967
23andMers786204967
23andMe allrs786204967
SNP Nexus

SNPshotrs786204967
SNPdbers786204967
MSV3drs786204967
GWAS Ctlgrs786204967
Max Magnitude0
ClinVar
Risk rs786204967(;)
Alt rs786204967(;)
Reference rs786204967(AG;AG)
Significance Pathogenic
Disease not provided
Variation info
Gene CDKL5
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.18622291_18622292delAG
CLNSRC RettBASE (CDKL5)
CLNACC RCV000169994.1,