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rs864309539

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864309539(C;T)
Make rs864309539(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position92956591
GeneCHD2
is asnp
is mentioned by
dbSNPrs864309539
ebirs864309539
HLIrs864309539
Exacrs864309539
Varsomers864309539
Maprs864309539
PheGenIrs864309539
hapmaprs864309539
1000 genomesrs864309539
hgdprs864309539
ensemblrs864309539
gopubmedrs864309539
geneviewrs864309539
scholarrs864309539
googlers864309539
pharmgkbrs864309539
gwascentralrs864309539
openSNPrs864309539
23andMers864309539
23andMe allrs864309539
SNP Nexus

SNPshotrs864309539
SNPdbers864309539
MSV3drs864309539
GWAS Ctlgrs864309539
Max Magnitude0
ClinVar
Risk rs864309539(T;T)
Alt rs864309539(T;T)
Reference rs864309539(C;C)
Significance Pathogenic
Disease Epileptic encephalopathy
Variation info
Gene CHD2
CLNDBN Epileptic encephalopathy, childhood-onset
Reversed 0
HGVS NC_000015.9:g.93499821C>T
CLNSRC
CLNACC RCV000202635.1,