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rs79761183

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs79761183(A;A)
Make rs79761183(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position52452776
GeneEFHC1
is asnp
is mentioned by
dbSNPrs79761183
ebirs79761183
HLIrs79761183
Exacrs79761183
Varsomers79761183
Maprs79761183
PheGenIrs79761183
hapmaprs79761183
1000 genomesrs79761183
hgdprs79761183
ensemblrs79761183
gopubmedrs79761183
geneviewrs79761183
scholarrs79761183
googlers79761183
pharmgkbrs79761183
gwascentralrs79761183
openSNPrs79761183
23andMers79761183
23andMe allrs79761183
SNP Nexus

SNPshotrs79761183
SNPdbers79761183
MSV3drs79761183
GWAS Ctlgrs79761183
GMAF0.004132
Max Magnitude0
OMIM608815
Desc
Variant0005
Relatedalso
ClinVar
Risk rs79761183(A;A)
Alt rs79761183(A;A)
Reference rs79761183(G;G)
Significance Other
Disease Myoclonic epilepsy not specified
Variation info
Gene EFHC1
CLNDBN Myoclonic epilepsy, juvenile 1 not specified
Reversed 0
HGVS NC_000006.11:g.52317574G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000002148.2, RCV000187341.1,