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rs7704909

From SNPedia

Orientationplus
Stabilizedplus
Make rs7704909(C;C)
Make rs7704909(C;T)
Make rs7704909(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position25898812
is asnp
is mentioned by
dbSNPrs7704909
ebirs7704909
HLIrs7704909
Exacrs7704909
Varsomers7704909
Maprs7704909
PheGenIrs7704909
hapmaprs7704909
1000 genomesrs7704909
hgdprs7704909
ensemblrs7704909
gopubmedrs7704909
geneviewrs7704909
scholarrs7704909
googlers7704909
pharmgkbrs7704909
gwascentralrs7704909
openSNPrs7704909
23andMers7704909
23andMe allrs7704909
SNP Nexus

SNPshotrs7704909
SNPdbers7704909
MSV3drs7704909
GWAS Ctlgrs7704909
GMAF0.2392
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19456320OA-icon.png] A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.


GET Evidence
rs7704909
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.229508
summary