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rs121434579

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs121434579(A;A)
Make rs121434579(A;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position161895774
GeneGABRA1
is asnp
is mentioned by
dbSNPrs121434579
ebirs121434579
HLIrs121434579
Exacrs121434579
Varsomers121434579
Maprs121434579
PheGenIrs121434579
hapmaprs121434579
1000 genomesrs121434579
hgdprs121434579
ensemblrs121434579
gopubmedrs121434579
geneviewrs121434579
scholarrs121434579
googlers121434579
pharmgkbrs121434579
gwascentralrs121434579
openSNPrs121434579
23andMers121434579
23andMe allrs121434579
SNP Nexus

SNPshotrs121434579
SNPdbers121434579
MSV3drs121434579
GWAS Ctlgrs121434579
Max Magnitude0
OMIM137160
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434579(A;A)
Alt rs121434579(A;A)
Reference rs121434579(C;C)
Significance Other
Disease Epilepsy
Variation info
Gene GABRA1
CLNDBN Epilepsy, juvenile myoclonic 5
Reversed 0
HGVS NC_000005.9:g.161322780C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017601.4,