NVL, nuclear VCP like, 4931

N. diseases: 8; N. variants: 8
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12565875
rs12565875
Entrez Id: 4931
Gene Symbol: NVL
NVL
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs1533589
rs1533589
Entrez Id: 4931
Gene Symbol: NVL
NVL
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs4654009
rs4654009
Entrez Id: 4931
Gene Symbol: NVL
NVL
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs4654009
rs4654009
Entrez Id: 4931
Gene Symbol: NVL
NVL
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs4654010
rs4654010
Entrez Id: 4931
Gene Symbol: NVL
NVL
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs4653579
rs4653579
Entrez Id: 4931
Gene Symbol: NVL
NVL
CUI: C0027051
Disease:
Myocardial Infarction
0.700 GeneticVariation GWASDB Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations. 21211798 2011
dbSNP: rs142293996
rs142293996
Entrez Id: 4931
Gene Symbol: NVL
NVL
CUI: C0011884
Disease:
Diabetic Retinopathy
0.010 GeneticVariation BEFREE After correction for multiple testing, the C allele of rs142293996 in an intron of nuclear VCP-like (<i>NVL</i>) was associated with DR in European discovery cohorts (<i>P</i> = 2.1 × 10<sup>-9</sup>), but did not reach genome-wide significance after meta-analysis with replication cohorts. 30487263 2019
dbSNP: rs10916583
rs10916583
Entrez Id: 4931
Gene Symbol: NVL
NVL
CUI: C0036341
Disease:
Schizophrenia
0.010 GeneticVariation BEFREE Furthermore, rs10916583 (adjusted P(allele) = 9.00E-03, adjusted P(genotype) = 3.15E-02, OR = 1.187) and rs16846649 (adjusted P(allele) = 8.92E-06, adjusted P(genotype) = 8.84E-05, OR = 0.653) remained strongly associated with the analysis of combined cases of major depressive disorder and schizophrenia after Bonferroni correction. 25891250 2015
dbSNP: rs16846649
rs16846649
Entrez Id: 4931
Gene Symbol: NVL
NVL
CUI: C0036341
Disease:
Schizophrenia
0.010 GeneticVariation BEFREE Furthermore, rs10916583 (adjusted P(allele) = 9.00E-03, adjusted P(genotype) = 3.15E-02, OR = 1.187) and rs16846649 (adjusted P(allele) = 8.92E-06, adjusted P(genotype) = 8.84E-05, OR = 0.653) remained strongly associated with the analysis of combined cases of major depressive disorder and schizophrenia after Bonferroni correction. 25891250 2015