CISD2, CDGSH iron sulfur domain 2, 493856

N. diseases: 106; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs223308
rs223308
Entrez Id: 150159;493856
Gene Symbol: SLC9B1;CISD2
SLC9B1;CISD2
CUI: C0017654
Disease:
Glomerular Filtration Rate
A 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs63749888
rs63749888
Entrez Id: 150159;493856
Gene Symbol: SLC9B1;CISD2
SLC9B1;CISD2
CUI: C1858028
Disease:
WOLFRAM SYNDROME 2
C 0.700 CausalMutation CLINVAR
dbSNP: rs223330
rs223330
Entrez Id: 493856
Gene Symbol: CISD2
CISD2
CUI: C0011265
Disease:
Presenile dementia
0.010 GeneticVariation BEFREE Two haplotype-tagging single nucleotide polymorphisms (htSNPs), rs223330 and rs223331, were selected from the CISD2 gene to test the association between their polymorphisms and the risk for dementia, and how ApoE ɛ4 status, sex, hypertension, and type 2 diabetes mellitus might modify this association. 26154755 2015
dbSNP: rs223330
rs223330
Entrez Id: 493856
Gene Symbol: CISD2
CISD2
CUI: C0497327
Disease:
Dementia
0.010 GeneticVariation BEFREE Two haplotype-tagging single nucleotide polymorphisms (htSNPs), rs223330 and rs223331, were selected from the CISD2 gene to test the association between their polymorphisms and the risk for dementia, and how ApoE ɛ4 status, sex, hypertension, and type 2 diabetes mellitus might modify this association. 26154755 2015
dbSNP: rs223330
rs223330
Entrez Id: 493856
Gene Symbol: CISD2
CISD2
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE Two haplotype-tagging single nucleotide polymorphisms (htSNPs), rs223330 and rs223331, were selected from the CISD2 gene to test the association between their polymorphisms and the risk for dementia, and how ApoE ɛ4 status, sex, hypertension, and type 2 diabetes mellitus might modify this association. 26154755 2015
dbSNP: rs223330
rs223330
Entrez Id: 493856
Gene Symbol: CISD2
CISD2
CUI: C0002395
Disease:
Alzheimer's Disease
0.010 GeneticVariation BEFREE rs223330 variant carriage was not associated with risk for AD [TT versus CC: adjusted odds ratio (AOR) = 0.98, 95% confidence interval (CI) = 0.59-1.62; TC versus CC: AOR = 0.72, 95% CI = 0.47-1.11]. 26154755 2015
dbSNP: rs223331
rs223331
Entrez Id: 493856
Gene Symbol: CISD2
CISD2
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE In addition, hypertension significantly modified the association between rs223331 and risk for AD (p = 0.005).Three common haplotypes (with a frequency of 99.8%) were observed for CISD2. 26154755 2015
dbSNP: rs223331
rs223331
Entrez Id: 493856
Gene Symbol: CISD2
CISD2
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE Two haplotype-tagging single nucleotide polymorphisms (htSNPs), rs223330 and rs223331, were selected from the CISD2 gene to test the association between their polymorphisms and the risk for dementia, and how ApoE ɛ4 status, sex, hypertension, and type 2 diabetes mellitus might modify this association. 26154755 2015
dbSNP: rs223331
rs223331
Entrez Id: 493856
Gene Symbol: CISD2
CISD2
CUI: C0002395
Disease:
Alzheimer's Disease
0.010 GeneticVariation BEFREE In addition, hypertension significantly modified the association between rs223331 and risk for AD (p = 0.005).Three common haplotypes (with a frequency of 99.8%) were observed for CISD2. 26154755 2015
dbSNP: rs223331
rs223331
Entrez Id: 493856
Gene Symbol: CISD2
CISD2
CUI: C0011265
Disease:
Presenile dementia
0.010 GeneticVariation BEFREE Two haplotype-tagging single nucleotide polymorphisms (htSNPs), rs223330 and rs223331, were selected from the CISD2 gene to test the association between their polymorphisms and the risk for dementia, and how ApoE ɛ4 status, sex, hypertension, and type 2 diabetes mellitus might modify this association. 26154755 2015
dbSNP: rs223331
rs223331
Entrez Id: 493856
Gene Symbol: CISD2
CISD2
CUI: C0497327
Disease:
Dementia
0.010 GeneticVariation BEFREE Two haplotype-tagging single nucleotide polymorphisms (htSNPs), rs223330 and rs223331, were selected from the CISD2 gene to test the association between their polymorphisms and the risk for dementia, and how ApoE ɛ4 status, sex, hypertension, and type 2 diabetes mellitus might modify this association. 26154755 2015