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rs864309534

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864309534(C;G)
Make rs864309534(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position92927284
GeneCHD2
is asnp
is mentioned by
dbSNPrs864309534
dbSNP (old)rs864309534
ClinGenrs864309534
ebirs864309534
HLIrs864309534
Exacrs864309534
Gnomadrs864309534
Varsomers864309534
Maprs864309534
PheGenIrs864309534
Biobankrs864309534
1000 genomesrs864309534
hgdprs864309534
ensemblrs864309534
gopubmedrs864309534
geneviewrs864309534
scholarrs864309534
googlers864309534
pharmgkbrs864309534
gwascentralrs864309534
openSNPrs864309534
23andMers864309534
23andMe allrs864309534
SNP Nexus

SNPshotrs864309534
SNPdbers864309534
MSV3drs864309534
GWAS Ctlgrs864309534
Max Magnitude0
ClinVar
Risk rs864309534(G;G)
Alt rs864309534(G;G)
Reference Rs864309534(C;C)
Significance Pathogenic
Disease Epileptic encephalopathy
Variation info
Gene CHD2
CLNDBN Epileptic encephalopathy, childhood-onset
Reversed 0
HGVS NC_000015.9:g.93470514C>G
CLNSRC
CLNACC RCV000202625.1,