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rs150447075

From SNPedia

Orientationplus
Stabilizedplus
Make rs150447075(G;G)
Make rs150447075(G;T)
Make rs150447075(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position146115955
GeneCNTNAP2
is asnp
is mentioned by
dbSNPrs150447075
dbSNP (old)rs150447075
ClinGenrs150447075
ebirs150447075
HLIrs150447075
Exacrs150447075
Gnomadrs150447075
Varsomers150447075
Maprs150447075
PheGenIrs150447075
Biobankrs150447075
1000 genomesrs150447075
hgdprs150447075
ensemblrs150447075
gopubmedrs150447075
geneviewrs150447075
scholarrs150447075
googlers150447075
pharmgkbrs150447075
gwascentralrs150447075
openSNPrs150447075
23andMers150447075
23andMe allrs150447075
SNP Nexus

SNPshotrs150447075
SNPdbers150447075
MSV3drs150447075
GWAS Ctlgrs150447075
Max Magnitude

[PMID 25224256] Variants of the CNTNAP2 5' promoter as risk factors for autism spectrum disorders: a genetic and functional approach