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rs60734921

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs60734921(C;T)
Make rs60734921(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position1202303
GeneCACNA1H
is asnp
is mentioned by
dbSNPrs60734921
ebirs60734921
HLIrs60734921
Exacrs60734921
Varsomers60734921
Maprs60734921
PheGenIrs60734921
hapmaprs60734921
1000 genomesrs60734921
hgdprs60734921
ensemblrs60734921
gopubmedrs60734921
geneviewrs60734921
scholarrs60734921
googlers60734921
pharmgkbrs60734921
gwascentralrs60734921
openSNPrs60734921
23andMers60734921
23andMe allrs60734921
SNP Nexus

SNPshotrs60734921
SNPdbers60734921
MSV3drs60734921
GWAS Ctlgrs60734921
GMAF0.0009183
Max Magnitude0
OMIM607904
Desc
Variant0005
Relatedalso


ClinVar
Risk rs60734921(T;T)
Alt rs60734921(T;T)
Reference rs60734921(C;C)
Significance Other
Disease Epilepsy
Variation info
Gene CACNA1H
CLNDBN Epilepsy, idiopathic generalized 6
Reversed 0
HGVS NC_000016.9:g.1252303C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002824.3,