Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs200913791
rs200913791
Entrez Id: 11186;51364
Gene Symbol: RASSF1;ZMYND10
RASSF1;ZMYND10
CUI: C3809543
Disease:
CILIARY DYSKINESIA, PRIMARY, 22
0.800 GeneticVariation UNIPROT ZMYND10 stabilizes intermediate chain proteins in the cytoplasmic pre-assembly of dynein arms. 29601588 2018
dbSNP: rs200913791
rs200913791
Entrez Id: 11186;51364
Gene Symbol: RASSF1;ZMYND10
RASSF1;ZMYND10
CUI: C3809543
Disease:
CILIARY DYSKINESIA, PRIMARY, 22
0.800 GeneticVariation UNIPROT Ciliary beat pattern and frequency in genetic variants of primary ciliary dyskinesia. 25186273 2014
dbSNP: rs200913791
rs200913791
Entrez Id: 11186;51364
Gene Symbol: RASSF1;ZMYND10
RASSF1;ZMYND10
CUI: C3809543
Disease:
CILIARY DYSKINESIA, PRIMARY, 22
0.800 GeneticVariation UNIPROT ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6. 23891469 2013
dbSNP: rs200913791
rs200913791
Entrez Id: 11186;51364
Gene Symbol: RASSF1;ZMYND10
RASSF1;ZMYND10
CUI: C3809543
Disease:
CILIARY DYSKINESIA, PRIMARY, 22
0.800 GeneticVariation UNIPROT Mutations in ZMYND10, a gene essential for proper axonemal assembly of inner and outer dynein arms in humans and flies, cause primary ciliary dyskinesia. 23891471 2013
dbSNP: rs200913791
rs200913791
Entrez Id: 11186;51364
Gene Symbol: RASSF1;ZMYND10
RASSF1;ZMYND10
CUI: C3809543
Disease:
CILIARY DYSKINESIA, PRIMARY, 22
G 0.800 CausalMutation CLINVAR
dbSNP: rs2073499
rs2073499
Entrez Id: 11186;102060282
Gene Symbol: RASSF1;RASSF1-AS1
RASSF1;RASSF1-AS1
CUI: C0036341
Disease:
Schizophrenia
G 0.700 GeneticVariation GWASCAT Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect. 30285260 2019
dbSNP: rs78166579
rs78166579
Entrez Id: 11186;51364
Gene Symbol: RASSF1;ZMYND10
RASSF1;ZMYND10
CUI: C0596887
Disease:
mathematical ability
T 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs2073499
rs2073499
Entrez Id: 11186;102060282
Gene Symbol: RASSF1;RASSF1-AS1
RASSF1;RASSF1-AS1
CUI: C0036341
Disease:
Schizophrenia
A 0.700 GeneticVariation GWASCAT Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia. 28991256 2017
dbSNP: rs1297857806
rs1297857806
Entrez Id: 11186;51364
Gene Symbol: RASSF1;ZMYND10
RASSF1;ZMYND10
CUI: C0008780
Disease:
Ciliary Motility Disorders
T 0.700 GeneticVariation CLINVAR Mutations in ZMYND10, a gene essential for proper axonemal assembly of inner and outer dynein arms in humans and flies, cause primary ciliary dyskinesia. 23891471 2013
dbSNP: rs1297857806
rs1297857806
Entrez Id: 11186;51364
Gene Symbol: RASSF1;ZMYND10
RASSF1;ZMYND10
CUI: C0008780
Disease:
Ciliary Motility Disorders
T 0.700 GeneticVariation CLINVAR ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6. 23891469 2013
dbSNP: rs200913791
rs200913791
Entrez Id: 11186;51364
Gene Symbol: RASSF1;ZMYND10
RASSF1;ZMYND10
CUI: C0008780
Disease:
Ciliary Motility Disorders
G 0.700 CausalMutation CLINVAR Mutations in ZMYND10, a gene essential for proper axonemal assembly of inner and outer dynein arms in humans and flies, cause primary ciliary dyskinesia. 23891471 2013
dbSNP: rs200913791
rs200913791
Entrez Id: 11186;51364
Gene Symbol: RASSF1;ZMYND10
RASSF1;ZMYND10
CUI: C4551906
Disease:
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
G 0.700 CausalMutation CLINVAR
dbSNP: rs397515460
rs397515460
Entrez Id: 11186;51364
Gene Symbol: RASSF1;ZMYND10
RASSF1;ZMYND10
CUI: C3809543
Disease:
CILIARY DYSKINESIA, PRIMARY, 22
A 0.700 CausalMutation CLINVAR
dbSNP: rs753061612
rs753061612
Entrez Id: 11186;51364
Gene Symbol: RASSF1;ZMYND10
RASSF1;ZMYND10
CUI: C3809543
Disease:
CILIARY DYSKINESIA, PRIMARY, 22
0.700 GeneticVariation UNIPROT
dbSNP: rs2073498
rs2073498
Entrez Id: 11186
Gene Symbol: RASSF1
RASSF1
CUI: C1306460
Disease:
Primary malignant neoplasm of lung
0.020 GeneticVariation BEFREE This meta-analysis suggests, for the first time, that RASSF1A Ala133Ser polymorphism may contribute to cancer susceptibility, especially for lung cancer. 24870779 2014
dbSNP: rs2073498
rs2073498
Entrez Id: 11186
Gene Symbol: RASSF1
RASSF1
CUI: C0684249
Disease:
Carcinoma of lung
0.020 GeneticVariation BEFREE This meta-analysis suggests, for the first time, that RASSF1A Ala133Ser polymorphism may contribute to cancer susceptibility, especially for lung cancer. 24870779 2014
dbSNP: rs2073498
rs2073498
Entrez Id: 11186
Gene Symbol: RASSF1
RASSF1
CUI: C0242379
Disease:
Malignant neoplasm of lung
0.020 GeneticVariation BEFREE This meta-analysis suggests, for the first time, that RASSF1A Ala133Ser polymorphism may contribute to cancer susceptibility, especially for lung cancer. 24870779 2014
dbSNP: rs2073498
rs2073498
Entrez Id: 11186
Gene Symbol: RASSF1
RASSF1
CUI: C1306459
Disease:
Primary malignant neoplasm
0.020 GeneticVariation BEFREE This meta-analysis suggests, for the first time, that RASSF1A Ala133Ser polymorphism may contribute to cancer susceptibility, especially for lung cancer. 24870779 2014
dbSNP: rs2073498
rs2073498
Entrez Id: 11186
Gene Symbol: RASSF1
RASSF1
CUI: C0006826
Disease:
Malignant Neoplasms
0.020 GeneticVariation BEFREE This meta-analysis suggests, for the first time, that RASSF1A Ala133Ser polymorphism may contribute to cancer susceptibility, especially for lung cancer. 24870779 2014
dbSNP: rs2073498
rs2073498
Entrez Id: 11186
Gene Symbol: RASSF1
RASSF1
CUI: C1306459
Disease:
Primary malignant neoplasm
0.020 GeneticVariation BEFREE A guanine (G)/thymine (T) common single nucleotide polymorphism (SNP) at first position of codon 133 in RASSF1A gene determines an alanine (Ala) to serine (Ser) (Ala133Ser) amino acidic substitution which may alter cancer risk by influencing the function of RASSF1A protein. 22394463 2012
dbSNP: rs2073498
rs2073498
Entrez Id: 11186
Gene Symbol: RASSF1
RASSF1
CUI: C0006826
Disease:
Malignant Neoplasms
0.020 GeneticVariation BEFREE A guanine (G)/thymine (T) common single nucleotide polymorphism (SNP) at first position of codon 133 in RASSF1A gene determines an alanine (Ala) to serine (Ser) (Ala133Ser) amino acidic substitution which may alter cancer risk by influencing the function of RASSF1A protein. 22394463 2012
dbSNP: rs2073498
rs2073498
Entrez Id: 11186
Gene Symbol: RASSF1
RASSF1
CUI: C0684249
Disease:
Carcinoma of lung
0.020 GeneticVariation BEFREE These results suggest that the RASSF1 Ala133Ser SNP is associated with development of lung cancer, especially of lung adenocarcinoma. 16125301 2006
dbSNP: rs2073498
rs2073498
Entrez Id: 11186
Gene Symbol: RASSF1
RASSF1
CUI: C1306460
Disease:
Primary malignant neoplasm of lung
0.020 GeneticVariation BEFREE These results suggest that the RASSF1 Ala133Ser SNP is associated with development of lung cancer, especially of lung adenocarcinoma. 16125301 2006
dbSNP: rs2073498
rs2073498
Entrez Id: 11186
Gene Symbol: RASSF1
RASSF1
CUI: C0242379
Disease:
Malignant neoplasm of lung
0.020 GeneticVariation BEFREE These results suggest that the RASSF1 Ala133Ser SNP is associated with development of lung cancer, especially of lung adenocarcinoma. 16125301 2006
dbSNP: rs1989839
rs1989839
Entrez Id: 11186;51364
Gene Symbol: RASSF1;ZMYND10
RASSF1;ZMYND10
CUI: C0027651
Disease:
Neoplasms
0.010 GeneticVariation BEFREE RESULTS In women in Southern China, the CT genotype of rs1989839 was associated with the patients with ovarian cancer (P=0.001), and was significantly correlated with tumor grade and stage (P=0.008). 29670073 2018