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rs2107856

From SNPedia

Orientationminus
Stabilizedminus
Make rs2107856(A;A)
Make rs2107856(A;C)
Make rs2107856(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position147491593
GeneCNTNAP2
is asnp
is mentioned by
dbSNPrs2107856
ebirs2107856
HLIrs2107856
Exacrs2107856
Varsomers2107856
Maprs2107856
PheGenIrs2107856
hapmaprs2107856
1000 genomesrs2107856
hgdprs2107856
ensemblrs2107856
gopubmedrs2107856
geneviewrs2107856
scholarrs2107856
googlers2107856
pharmgkbrs2107856
gwascentralrs2107856
openSNPrs2107856
23andMers2107856
23andMe allrs2107856
SNP Nexus

SNPshotrs2107856
SNPdbers2107856
MSV3drs2107856
GWAS Ctlgrs2107856
GMAF0.3287
Max Magnitude
? (A;A) (A;C) (C;C) 28
[PMID 20808326OA-icon.png] Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome