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rs121909673

From SNPedia

Orientationplus
Stabilizedplus
Make rs121909673(A;A)
Make rs121909673(A;G)
Make rs121909673(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position162093965
GeneGABRG2
is asnp
is mentioned by
dbSNPrs121909673
dbSNP (old)rs121909673
ClinGenrs121909673
ebirs121909673
HLIrs121909673
Exacrs121909673
Gnomadrs121909673
Varsomers121909673
Maprs121909673
PheGenIrs121909673
Biobankrs121909673
1000 genomesrs121909673
hgdprs121909673
ensemblrs121909673
gopubmedrs121909673
geneviewrs121909673
scholarrs121909673
googlers121909673
pharmgkbrs121909673
gwascentralrs121909673
openSNPrs121909673
23andMers121909673
23andMe allrs121909673
SNP Nexus

SNPshotrs121909673
SNPdbers121909673
MSV3drs121909673
GWAS Ctlgrs121909673
Merged fromRs28933070
Max Magnitude
OMIM137164
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121909673(A;A)
Alt rs121909673(A;A)
Reference rs121909673(G;G)
Significance Other
Disease Epilepsy Familial febrile seizures 8 not provided
Variation info
Gene GABRG2
CLNDBN Epilepsy, childhood absence 2 Familial febrile seizures 8 not provided
Reversed 0
HGVS NC_000005.9:g.161520971G>A
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000017592.4, RCV000017593.29, RCV000187520.2,