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rs121909269

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121909269(A;A)
Make rs121909269(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position122284647
GeneCASR
is asnp
is mentioned by
dbSNPrs121909269
ebirs121909269
HLIrs121909269
Exacrs121909269
Varsomers121909269
Maprs121909269
PheGenIrs121909269
hapmaprs121909269
1000 genomesrs121909269
hgdprs121909269
ensemblrs121909269
gopubmedrs121909269
geneviewrs121909269
scholarrs121909269
googlers121909269
pharmgkbrs121909269
gwascentralrs121909269
openSNPrs121909269
23andMers121909269
23andMe allrs121909269
SNP Nexus

SNPshotrs121909269
SNPdbers121909269
MSV3drs121909269
GWAS Ctlgrs121909269
Max Magnitude0
OMIM601199
Desc
Variant0050
Relatedalso
ClinVar
Risk rs121909269(A;A)
Alt rs121909269(A;A)
Reference rs121909269(G;G)
Significance Other
Disease Epilepsy
Variation info
Gene CASR
CLNDBN Epilepsy, idiopathic generalized 8
Reversed 0
HGVS NC_000003.11:g.122003494G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008864.3,