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rs878854144

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878854144(-;-)
Make rs878854144(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position162097840
GeneGABRG2
is asnp
is mentioned by
dbSNPrs878854144
ebirs878854144
HLIrs878854144
Exacrs878854144
Varsomers878854144
Maprs878854144
PheGenIrs878854144
hapmaprs878854144
1000 genomesrs878854144
hgdprs878854144
ensemblrs878854144
gopubmedrs878854144
geneviewrs878854144
scholarrs878854144
googlers878854144
pharmgkbrs878854144
gwascentralrs878854144
openSNPrs878854144
23andMers878854144
23andMe allrs878854144
SNP Nexus

SNPshotrs878854144
SNPdbers878854144
MSV3drs878854144
GWAS Ctlgrs878854144
Max Magnitude0
ClinVar
Risk rs878854144(;)
Alt rs878854144(;)
Reference rs878854144(G;G)
Significance Pathogenic
Disease Epilepsy Familial febrile seizures 8
Variation info
Gene GABRG2
CLNDBN Epilepsy, childhood absence 2 Familial febrile seizures 8
Reversed 0
HGVS NC_000005.9:g.161524846delG
CLNSRC
CLNACC RCV000227482.1,