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rs864309540

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864309540(C;C)
Make rs864309540(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position92972380
GeneCHD2
is asnp
is mentioned by
dbSNPrs864309540
ebirs864309540
HLIrs864309540
Exacrs864309540
Varsomers864309540
Maprs864309540
PheGenIrs864309540
hapmaprs864309540
1000 genomesrs864309540
hgdprs864309540
ensemblrs864309540
gopubmedrs864309540
geneviewrs864309540
scholarrs864309540
googlers864309540
pharmgkbrs864309540
gwascentralrs864309540
openSNPrs864309540
23andMers864309540
23andMe allrs864309540
SNP Nexus

SNPshotrs864309540
SNPdbers864309540
MSV3drs864309540
GWAS Ctlgrs864309540
Max Magnitude0
ClinVar
Risk rs864309540(C;C)
Alt rs864309540(C;C)
Reference rs864309540(T;T)
Significance Pathogenic
Disease Epileptic encephalopathy
Variation info
Gene CHD2
CLNDBN Epileptic encephalopathy, childhood-onset
Reversed 0
HGVS NC_000015.9:g.93515610T>C
CLNSRC
CLNACC RCV000202644.1,