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rs119454947

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs119454947(A;A)
Make rs119454947(A;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position1195503
GeneCACNA1H
is asnp
is mentioned by
dbSNPrs119454947
ebirs119454947
HLIrs119454947
Exacrs119454947
Varsomers119454947
Maprs119454947
PheGenIrs119454947
hapmaprs119454947
1000 genomesrs119454947
hgdprs119454947
ensemblrs119454947
gopubmedrs119454947
geneviewrs119454947
scholarrs119454947
googlers119454947
pharmgkbrs119454947
gwascentralrs119454947
openSNPrs119454947
23andMers119454947
23andMe allrs119454947
SNP Nexus

SNPshotrs119454947
SNPdbers119454947
MSV3drs119454947
GWAS Ctlgrs119454947
Max Magnitude0
OMIM607904
Desc
Variant0001
Relatedalso
ClinVar
Risk rs119454947(A,G,T;A,G,T)
Alt rs119454947(A,G,T;A,G,T)
Reference rs119454947(C;C)
Significance Other
Disease Epilepsy
Variation info
Gene CACNA1H
CLNDBN Epilepsy, childhood absence 6
Reversed 0
HGVS NC_000016.9:g.1245503C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000002820.2,