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rs270102

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs270102(A;G)
Make rs270102(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position25109771
is asnp
is mentioned by
dbSNPrs270102
ebirs270102
HLIrs270102
Exacrs270102
Varsomers270102
Maprs270102
PheGenIrs270102
hapmaprs270102
1000 genomesrs270102
hgdprs270102
ensemblrs270102
gopubmedrs270102
geneviewrs270102
scholarrs270102
googlers270102
pharmgkbrs270102
gwascentralrs270102
openSNPrs270102
23andMers270102
23andMe allrs270102
SNP Nexus

SNPshotrs270102
SNPdbers270102
MSV3drs270102
GWAS Ctlgrs270102
Max Magnitude0
OMIM604569
DescCONTACTIN-ASSOCIATED PROTEIN-LIKE 2; CNTNAP2
Variant
Relatedalso
OMIM612100
Desc
Variant
Relatedalso
[PMID 19456320OA-icon.png] A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.