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rs6660197

From SNPedia

Orientationplus
Stabilizedplus
Make rs6660197(C;C)
Make rs6660197(C;T)
Make rs6660197(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position200734413
is asnp
is mentioned by
dbSNPrs6660197
ebirs6660197
HLIrs6660197
Exacrs6660197
Varsomers6660197
Maprs6660197
PheGenIrs6660197
hapmaprs6660197
1000 genomesrs6660197
hgdprs6660197
ensemblrs6660197
gopubmedrs6660197
geneviewrs6660197
scholarrs6660197
googlers6660197
pharmgkbrs6660197
gwascentralrs6660197
openSNPrs6660197
23andMers6660197
23andMe allrs6660197
SNP Nexus

SNPshotrs6660197
SNPdbers6660197
MSV3drs6660197
GWAS Ctlgrs6660197
GMAF0.146
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 22116939] Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese