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rs864309545

From SNPedia

Orientationplus
Make rs864309545(-;-)
Make rs864309545(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position93014723
GeneCHD2
is asnp
is mentioned by
dbSNPrs864309545
ebirs864309545
HLIrs864309545
Exacrs864309545
Varsomers864309545
Maprs864309545
PheGenIrs864309545
hapmaprs864309545
1000 genomesrs864309545
hgdprs864309545
ensemblrs864309545
gopubmedrs864309545
geneviewrs864309545
scholarrs864309545
googlers864309545
pharmgkbrs864309545
gwascentralrs864309545
openSNPrs864309545
23andMers864309545
23andMe allrs864309545
SNP Nexus

SNPshotrs864309545
SNPdbers864309545
MSV3drs864309545
GWAS Ctlgrs864309545
Max Magnitude
ClinVar
Risk rs864309545(;)
Alt rs864309545(;)
Reference rs864309545(G;G)
Significance Pathogenic
Disease Epileptic encephalopathy
Variation info
Gene CHD2
CLNDBN Epileptic encephalopathy, childhood-onset
Reversed 0
HGVS NC_000015.9:g.93557953delG
CLNSRC
CLNACC RCV000202621.1,