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rs10447760

From SNPedia

Orientationplus
Stabilizedplus
Make rs10447760(C;C)
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ReferenceGRCh38.p7 38.3/150
Chromosome7
Position114083210
is asnp
is mentioned by
dbSNPrs10447760
dbSNP (old)rs10447760
ClinGenrs10447760
ebirs10447760
HLIrs10447760
Exacrs10447760
Gnomadrs10447760
Varsomers10447760
Maprs10447760
PheGenIrs10447760
Biobankrs10447760
1000 genomesrs10447760
hgdprs10447760
ensemblrs10447760
gopubmedrs10447760
geneviewrs10447760
scholarrs10447760
googlers10447760
pharmgkbrs10447760
gwascentralrs10447760
openSNPrs10447760
23andMers10447760
23andMe allrs10447760
SNPshotrs10447760
SNPdbers10447760
MSV3drs10447760
GWAS Ctlgrs10447760
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 29346177] No association between FOXP2 rs10447760 and schizophrenia in a replication study of the Chinese Han population.