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rs1445442

From SNPedia

Orientationplus
Stabilizedplus
Make rs1445442(A;A)
Make rs1445442(A;G)
Make rs1445442(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position64897514
GenePVRIG
is asnp
is mentioned by
dbSNPrs1445442
ebirs1445442
HLIrs1445442
Exacrs1445442
Varsomers1445442
Maprs1445442
PheGenIrs1445442
hapmaprs1445442
1000 genomesrs1445442
hgdprs1445442
ensemblrs1445442
gopubmedrs1445442
geneviewrs1445442
scholarrs1445442
googlers1445442
pharmgkbrs1445442
gwascentralrs1445442
openSNPrs1445442
23andMers1445442
23andMe allrs1445442
SNP Nexus

SNPshotrs1445442
SNPdbers1445442
MSV3drs1445442
GWAS Ctlgrs1445442
GMAF0.3848
Max Magnitude
? (A;A) (A;G) (G;G) 28
OMIM610908
DescAUTISM, SUSCEPTIBILITY TO, 13; AUTS13
Variant
Relatedalso


[PMID 17179998] Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.