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rs10244837

From SNPedia

Orientationplus
Stabilizedplus
Make rs10244837(A;A)
Make rs10244837(A;G)
Make rs10244837(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position146778222
GeneCNTNAP2
is asnp
is mentioned by
dbSNPrs10244837
ebirs10244837
HLIrs10244837
Exacrs10244837
Varsomers10244837
Maprs10244837
PheGenIrs10244837
hapmaprs10244837
1000 genomesrs10244837
hgdprs10244837
ensemblrs10244837
gopubmedrs10244837
geneviewrs10244837
scholarrs10244837
googlers10244837
pharmgkbrs10244837
gwascentralrs10244837
openSNPrs10244837
23andMers10244837
23andMe allrs10244837
SNP Nexus

SNPshotrs10244837
SNPdbers10244837
MSV3drs10244837
GWAS Ctlgrs10244837
GMAF0.4545
Max Magnitude
? (A;A) (A;G) (G;G) 28

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