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rs864309548

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864309548(C;T)
Make rs864309548(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position93020026
GeneCHD2
is asnp
is mentioned by
dbSNPrs864309548
ebirs864309548
HLIrs864309548
Exacrs864309548
Varsomers864309548
Maprs864309548
PheGenIrs864309548
hapmaprs864309548
1000 genomesrs864309548
hgdprs864309548
ensemblrs864309548
gopubmedrs864309548
geneviewrs864309548
scholarrs864309548
googlers864309548
pharmgkbrs864309548
gwascentralrs864309548
openSNPrs864309548
23andMers864309548
23andMe allrs864309548
SNP Nexus

SNPshotrs864309548
SNPdbers864309548
MSV3drs864309548
GWAS Ctlgrs864309548
Max Magnitude0
ClinVar
Risk rs864309548(T;T)
Alt rs864309548(T;T)
Reference rs864309548(C;C)
Significance Pathogenic
Disease Epileptic encephalopathy
Variation info
Gene CHD2
CLNDBN Epileptic encephalopathy, childhood-onset
Reversed 0
HGVS NC_000015.9:g.93563256C>T
CLNSRC
CLNACC RCV000202641.1,