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rs4327572

From SNPedia

Orientationplus
Stabilizedplus
Make rs4327572(C;C)
Make rs4327572(C;T)
Make rs4327572(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position25972712
is asnp
is mentioned by
dbSNPrs4327572
ebirs4327572
HLIrs4327572
Exacrs4327572
Varsomers4327572
Maprs4327572
PheGenIrs4327572
hapmaprs4327572
1000 genomesrs4327572
hgdprs4327572
ensemblrs4327572
gopubmedrs4327572
geneviewrs4327572
scholarrs4327572
googlers4327572
pharmgkbrs4327572
gwascentralrs4327572
openSNPrs4327572
23andMers4327572
23andMe allrs4327572
SNP Nexus

SNPshotrs4327572
SNPdbers4327572
MSV3drs4327572
GWAS Ctlgrs4327572
GMAF0.2397
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
rs4327572
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.234375
summary