Have questions? Visit https://www.reddit.com/r/SNPedia

rs864309542

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864309542(C;T)
Make rs864309542(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position92978381
GeneCHD2
is asnp
is mentioned by
dbSNPrs864309542
ebirs864309542
HLIrs864309542
Exacrs864309542
Varsomers864309542
Maprs864309542
PheGenIrs864309542
hapmaprs864309542
1000 genomesrs864309542
hgdprs864309542
ensemblrs864309542
gopubmedrs864309542
geneviewrs864309542
scholarrs864309542
googlers864309542
pharmgkbrs864309542
gwascentralrs864309542
openSNPrs864309542
23andMers864309542
23andMe allrs864309542
SNP Nexus

SNPshotrs864309542
SNPdbers864309542
MSV3drs864309542
GWAS Ctlgrs864309542
Max Magnitude0
ClinVar
Risk rs864309542(T;T)
Alt rs864309542(T;T)
Reference rs864309542(C;C)
Significance Pathogenic
Disease Epileptic encephalopathy
Variation info
Gene CHD2
CLNDBN Epileptic encephalopathy, childhood-onset
Reversed 0
HGVS NC_000015.9:g.93521611C>T
CLNSRC
CLNACC RCV000202637.1,