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rs2228638

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0
Make rs2228638(A;A)
Make rs2228638(A;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position33186354
GeneNRP1
is asnp
is mentioned by
dbSNPrs2228638
dbSNP (classic)rs2228638
ClinGenrs2228638
ebirs2228638
HLIrs2228638
Exacrs2228638
Gnomadrs2228638
Varsomers2228638
LitVarrs2228638
Maprs2228638
PheGenIrs2228638
Biobankrs2228638
1000 genomesrs2228638
hgdprs2228638
ensemblrs2228638
geneviewrs2228638
scholarrs2228638
googlers2228638
pharmgkbrs2228638
gwascentralrs2228638
openSNPrs2228638
23andMers2228638
SNPshotrs2228638
SNPdbers2228638
MSV3drs2228638
GWAS Ctlgrs2228638
GMAF0.09642
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 23297363OA-icon.png]
Trait Tetralogy of Fallot
Title Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot.
Risk Allele A
P-val 2E-7
Odds Ratio 1.45 [1.239-1.69]


[PMID 16385451OA-icon.png] A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.


[PMID 29432830] Functional polymorphisms of the neuropilin 1 gene are associated with the risk of tetralogy of Fallot in a Chinese Han population.