NRP2, neuropilin 2, 8828

N. diseases: 144; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs16837641
rs16837641
Entrez Id: 8828
Gene Symbol: NRP2
NRP2
CUI: C2985280
Disease:
Blood Protein Measurement 		G 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs16837641
rs16837641
Entrez Id: 8828
Gene Symbol: NRP2
NRP2
CUI: C2985280
Disease:
Blood Protein Measurement 		A 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs779617179
rs779617179
Entrez Id: 8828
Gene Symbol: NRP2
NRP2
CUI: C0000772
Disease:
Multiple congenital anomalies 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs849563
rs849563
Entrez Id: 8828
Gene Symbol: NRP2
NRP2
CUI: C0004352
Disease:
Autistic Disorder 		0.020 GeneticVariation BEFREE The results of this study showed that there is a significant association between rs849563 polymorphism and autism in the studied population. 28484884 2017
dbSNP: rs849563
rs849563
Entrez Id: 8828
Gene Symbol: NRP2
NRP2
CUI: C0004352
Disease:
Autistic Disorder 		0.020 GeneticVariation BEFREE We found significant genetic association between autism and two of the SNPs of the NRP2 gene (rs849578: P = 0.017, rs849563: P = 0.027), as well as specific haplotypes, especially those formed by rs849563. 17427189 2007
dbSNP: rs849578
rs849578
Entrez Id: 8828
Gene Symbol: NRP2
NRP2
CUI: C0004352
Disease:
Autistic Disorder 		0.010 GeneticVariation BEFREE We found significant genetic association between autism and two of the SNPs of the NRP2 gene (rs849578: P = 0.017, rs849563: P = 0.027), as well as specific haplotypes, especially those formed by rs849563. 17427189 2007