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rs398122998

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122998(A;A)
Make rs398122998(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position93020076
GeneCHD2
is asnp
is mentioned by
dbSNPrs398122998
ebirs398122998
HLIrs398122998
Exacrs398122998
Varsomers398122998
Maprs398122998
PheGenIrs398122998
hapmaprs398122998
1000 genomesrs398122998
hgdprs398122998
ensemblrs398122998
gopubmedrs398122998
geneviewrs398122998
scholarrs398122998
googlers398122998
pharmgkbrs398122998
gwascentralrs398122998
openSNPrs398122998
23andMers398122998
23andMe allrs398122998
SNP Nexus

SNPshotrs398122998
SNPdbers398122998
MSV3drs398122998
GWAS Ctlgrs398122998
Max Magnitude0
ClinVar
Risk rs398122998(A;A)
Alt rs398122998(A;A)
Reference rs398122998(G;G)
Significance Pathogenic
Disease Epileptic encephalopathy
Variation info
Gene CHD2
CLNDBN Epileptic encephalopathy, childhood-onset
Reversed 0
HGVS NC_000015.9:g.93563306G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000077771.3,