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rs1130496

From SNPedia
Orientationminus
Stabilizedminus
Make rs1130496(A;A)
Make rs1130496(A;G)
Make rs1130496(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position158167203
GenePTPRN2
is asnp
is mentioned by
dbSNPrs1130496
dbSNP (old)rs1130496
ClinGenrs1130496
ebirs1130496
HLIrs1130496
Exacrs1130496
Gnomadrs1130496
Varsomers1130496
Maprs1130496
PheGenIrs1130496
Biobankrs1130496
1000 genomesrs1130496
hgdprs1130496
ensemblrs1130496
gopubmedrs1130496
geneviewrs1130496
scholarrs1130496
googlers1130496
pharmgkbrs1130496
gwascentralrs1130496
openSNPrs1130496
23andMers1130496
23andMe allrs1130496
SNPshotrs1130496
SNPdbers1130496
MSV3drs1130496
GWAS Ctlgrs1130496
GMAF0.3526
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19456320OA-icon.png] A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.