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rs864309541

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs864309541(A;G)
Make rs864309541(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position92974940
GeneCHD2
is asnp
is mentioned by
dbSNPrs864309541
ebirs864309541
HLIrs864309541
Exacrs864309541
Varsomers864309541
Maprs864309541
PheGenIrs864309541
hapmaprs864309541
1000 genomesrs864309541
hgdprs864309541
ensemblrs864309541
gopubmedrs864309541
geneviewrs864309541
scholarrs864309541
googlers864309541
pharmgkbrs864309541
gwascentralrs864309541
openSNPrs864309541
23andMers864309541
23andMe allrs864309541
SNP Nexus

SNPshotrs864309541
SNPdbers864309541
MSV3drs864309541
GWAS Ctlgrs864309541
Max Magnitude0
ClinVar
Risk rs864309541(G;G)
Alt rs864309541(G;G)
Reference rs864309541(A;A)
Significance Pathogenic
Disease Epileptic encephalopathy
Variation info
Gene CHD2
CLNDBN Epileptic encephalopathy, childhood-onset
Reversed 0
HGVS NC_000015.9:g.93518170A>G
CLNSRC
CLNACC RCV000202629.1,