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rs119454948

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs119454948(A;A)
Make rs119454948(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position1200296
GeneCACNA1H
is asnp
is mentioned by
dbSNPrs119454948
ebirs119454948
HLIrs119454948
Exacrs119454948
Varsomers119454948
Maprs119454948
PheGenIrs119454948
hapmaprs119454948
1000 genomesrs119454948
hgdprs119454948
ensemblrs119454948
gopubmedrs119454948
geneviewrs119454948
scholarrs119454948
googlers119454948
pharmgkbrs119454948
gwascentralrs119454948
openSNPrs119454948
23andMers119454948
23andMe allrs119454948
SNP Nexus

SNPshotrs119454948
SNPdbers119454948
MSV3drs119454948
GWAS Ctlgrs119454948
Max Magnitude0
OMIM607904
Desc
Variant0002
Relatedalso
ClinVar
Risk rs119454948(A;A)
Alt rs119454948(A;A)
Reference rs119454948(G;G)
Significance Other
Disease Epilepsy
Variation info
Gene CACNA1H
CLNDBN Epilepsy, childhood absence 6
Reversed 0
HGVS NC_000016.9:g.1250296G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000002821.2,