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rs267606837

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606837(C;G)
Make rs267606837(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position162097839
GeneGABRG2
is asnp
is mentioned by
dbSNPrs267606837
ebirs267606837
HLIrs267606837
Exacrs267606837
Varsomers267606837
Maprs267606837
PheGenIrs267606837
hapmaprs267606837
1000 genomesrs267606837
hgdprs267606837
ensemblrs267606837
gopubmedrs267606837
geneviewrs267606837
scholarrs267606837
googlers267606837
pharmgkbrs267606837
gwascentralrs267606837
openSNPrs267606837
23andMers267606837
23andMe allrs267606837
SNP Nexus

SNPshotrs267606837
SNPdbers267606837
MSV3drs267606837
GWAS Ctlgrs267606837
Max Magnitude0
ClinVar
Risk rs267606837(G;G)
Alt rs267606837(G;G)
Reference rs267606837(C;C)
Significance Pathogenic
Disease Familial febrile seizures 8
Variation info
Gene GABRG2
CLNDBN Familial febrile seizures 8
Reversed 0
HGVS NC_000005.9:g.161524845C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000017597.27,