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

rs864309535

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs864309535(-;T)
Make rs864309535(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position92949025
GeneCHD2
is asnp
is mentioned by
dbSNPrs864309535
ClinGenrs864309535
ebirs864309535
HLIrs864309535
Exacrs864309535
Varsomers864309535
Maprs864309535
PheGenIrs864309535
hapmaprs864309535
1000 genomesrs864309535
hgdprs864309535
ensemblrs864309535
gopubmedrs864309535
geneviewrs864309535
scholarrs864309535
googlers864309535
pharmgkbrs864309535
gwascentralrs864309535
openSNPrs864309535
23andMers864309535
23andMe allrs864309535
SNP Nexus

SNPshotrs864309535
SNPdbers864309535
MSV3drs864309535
GWAS Ctlgrs864309535
Max Magnitude0
ClinVar
Risk rs864309535(T;T)
Alt rs864309535(T;T)
Reference Rs864309535(;)
Significance Pathogenic
Disease Epileptic encephalopathy
Variation info
Gene CHD2
CLNDBN Epileptic encephalopathy, childhood-onset
Reversed 0
HGVS NC_000015.9:g.93492255dupT
CLNSRC
CLNACC RCV000202624.1,