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rs2292096

From SNPedia

Orientationplus
Stabilizedplus
Make rs2292096(A;A)
Make rs2292096(A;G)
Make rs2292096(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position200857641
GeneCAMSAP1L1
is asnp
is mentioned by
dbSNPrs2292096
ebirs2292096
HLIrs2292096
Exacrs2292096
Varsomers2292096
Maprs2292096
PheGenIrs2292096
hapmaprs2292096
1000 genomesrs2292096
hgdprs2292096
ensemblrs2292096
gopubmedrs2292096
geneviewrs2292096
scholarrs2292096
googlers2292096
pharmgkbrs2292096
gwascentralrs2292096
openSNPrs2292096
23andMers2292096
23andMe allrs2292096
SNP Nexus

SNPshotrs2292096
SNPdbers2292096
MSV3drs2292096
GWAS Ctlgrs2292096
GMAF0.1515
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22116939]
Trait
Title Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese.
Risk Allele
P-val 1E-8
Odds Ratio 1.5900 None


[PMID 24148305] The potential role of CAMSAP1L1 in symptomatic epilepsy