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rs1805032

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1805032(C;T)
Make rs1805032(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position151839238
GeneCACNB4
is asnp
is mentioned by
dbSNPrs1805032
ebirs1805032
HLIrs1805032
Exacrs1805032
Varsomers1805032
Maprs1805032
PheGenIrs1805032
hapmaprs1805032
1000 genomesrs1805032
hgdprs1805032
ensemblrs1805032
gopubmedrs1805032
geneviewrs1805032
scholarrs1805032
googlers1805032
pharmgkbrs1805032
gwascentralrs1805032
openSNPrs1805032
23andMers1805032
23andMe allrs1805032
SNP Nexus

SNPshotrs1805032
SNPdbers1805032
MSV3drs1805032
GWAS Ctlgrs1805032
Max Magnitude0
OMIM601949
Desc
Variant0001
Relatedalso
ClinVar
Risk rs1805032(T;T)
Alt rs1805032(T;T)
Reference rs1805032(C;C)
Significance Other
Disease Epilepsy
Variation info
Gene CACNB4
CLNDBN Epilepsy, juvenile myoclonic 6
Reversed 1
HGVS NC_000002.11:g.152695752G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008045.2,