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rs1718101

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0
Make rs1718101(A;A)
Make rs1718101(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position146425696
GeneCNTNAP2
is asnp
is mentioned by
dbSNPrs1718101
ebirs1718101
HLIrs1718101
Exacrs1718101
Varsomers1718101
Maprs1718101
PheGenIrs1718101
hapmaprs1718101
1000 genomesrs1718101
hgdprs1718101
ensemblrs1718101
gopubmedrs1718101
geneviewrs1718101
scholarrs1718101
googlers1718101
pharmgkbrs1718101
gwascentralrs1718101
openSNPrs1718101
23andMers1718101
23andMe allrs1718101
SNP Nexus

SNPshotrs1718101
SNPdbers1718101
MSV3drs1718101
GWAS Ctlgrs1718101
GMAF0.02204
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 22843504OA-icon.png] Individual common variants exert weak effects on risk for Autism Spectrum Disorders