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rs2141388

From SNPedia

Orientationplus
Stabilizedplus
Make rs2141388(C;C)
Make rs2141388(C;T)
Make rs2141388(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position147492648
GeneCNTNAP2
is asnp
is mentioned by
dbSNPrs2141388
ebirs2141388
HLIrs2141388
Exacrs2141388
Varsomers2141388
Maprs2141388
PheGenIrs2141388
hapmaprs2141388
1000 genomesrs2141388
hgdprs2141388
ensemblrs2141388
gopubmedrs2141388
geneviewrs2141388
scholarrs2141388
googlers2141388
pharmgkbrs2141388
gwascentralrs2141388
openSNPrs2141388
23andMers2141388
23andMe allrs2141388
SNP Nexus

SNPshotrs2141388
SNPdbers2141388
MSV3drs2141388
GWAS Ctlgrs2141388
GMAF0.3287
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 20808326OA-icon.png] Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome