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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
ebirs1130496
HLIrs1130496
Exacrs1130496
Varsomers1130496
Maprs1130496
PheGenIrs1130496
hapmaprs1130496
1000 genomesrs1130496
hgdprs1130496
ensemblrs1130496
gopubmedrs1130496
geneviewrs1130496
scholarrs1130496
googlers1130496
pharmgkbrs1130496
gwascentralrs1130496
openSNPrs1130496
23andMers1130496
23andMe allrs1130496
SNP Nexus

SNPshotrs1130496
SNPdbers1130496
MSV3drs1130496
GWAS Ctlgrs1130496
GMAF0.3526
Max Magnitude
? (A;A) (A;G) (G;G) 28
Venter snp
Source plos
Gene PTPRN2
allele T
frequency
sift TOLERATED
HuRef 1103652756970
Disease Association Autoantigen in insulin-dependent diabetes mellitus (IDDM).



Neighborrs1130495
Distance16
[PMID 19456320OA-icon.png] A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.


GET Evidence
PTPRN2-R213H
aa_change Arg213His
aa_change_short R213H
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.342849
summary