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rs794726897

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794726897(C;T)
Make rs794726897(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100407784
GenePCDH19
is asnp
is mentioned by
dbSNPrs794726897
ebirs794726897
HLIrs794726897
Exacrs794726897
Varsomers794726897
Maprs794726897
PheGenIrs794726897
hapmaprs794726897
1000 genomesrs794726897
hgdprs794726897
ensemblrs794726897
gopubmedrs794726897
geneviewrs794726897
scholarrs794726897
googlers794726897
pharmgkbrs794726897
gwascentralrs794726897
openSNPrs794726897
23andMers794726897
23andMe allrs794726897
SNP Nexus

SNPshotrs794726897
SNPdbers794726897
MSV3drs794726897
GWAS Ctlgrs794726897
Max Magnitude0
ClinVar
Risk rs794726897(T;T)
Alt rs794726897(T;T)
Reference rs794726897(C;C)
Significance Pathogenic
Disease Early infantile epileptic encephalopathy 9
Variation info
Gene PCDH19
CLNDBN Early infantile epileptic encephalopathy 9
Reversed 1
HGVS NC_000023.10:g.99662782G>A
CLNSRC
CLNACC RCV000173238.1,