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rs10500171

From SNPedia

Orientationplus
Stabilizedplus
Make rs10500171(A;A)
Make rs10500171(A;G)
Make rs10500171(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position147183313
GeneCNTNAP2
is asnp
is mentioned by
dbSNPrs10500171
ebirs10500171
HLIrs10500171
Exacrs10500171
Varsomers10500171
Maprs10500171
PheGenIrs10500171
hapmaprs10500171
1000 genomesrs10500171
hgdprs10500171
ensemblrs10500171
gopubmedrs10500171
geneviewrs10500171
scholarrs10500171
googlers10500171
pharmgkbrs10500171
gwascentralrs10500171
openSNPrs10500171
23andMers10500171
23andMe allrs10500171
SNP Nexus

SNPshotrs10500171
SNPdbers10500171
MSV3drs10500171
GWAS Ctlgrs10500171
GMAF0.4495
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 20414140] Association analysis of CNTNAP2 polymorphisms with autism in the Chinese Han population