Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10770705
rs10770705
Entrez Id: 53919
Gene Symbol: SLCO1C1
SLCO1C1
CUI: C0005890
Disease:
Body Height
A 0.700 GeneticVariation GWASCAT Defining the role of common variation in the genomic and biological architecture of adult human height. 25282103 2014
dbSNP: rs10770705
rs10770705
Entrez Id: 53919
Gene Symbol: SLCO1C1
SLCO1C1
CUI: C0489786
Disease:
Height
A 0.700 GeneticVariation GWASDB Hundreds of variants clustered in genomic loci and biological pathways affect human height. 20881960 2010
dbSNP: rs10770705
rs10770705
Entrez Id: 53919
Gene Symbol: SLCO1C1
SLCO1C1
CUI: C0005890
Disease:
Body Height
A 0.700 GeneticVariation GWASCAT Hundreds of variants clustered in genomic loci and biological pathways affect human height. 20881960 2010
dbSNP: rs974453
rs974453
Entrez Id: 53919
Gene Symbol: SLCO1C1
SLCO1C1
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE In the AMI cohort, associations between: DIO1 rs12095080 and hypertension; DIO2 rs225015 and diabetes mellitus; and the OATP1C1 rs974453 genotype, and AMI type were established. 29641285 2018
dbSNP: rs974453
rs974453
Entrez Id: 53919
Gene Symbol: SLCO1C1
SLCO1C1
CUI: C0011849
Disease:
Diabetes Mellitus
0.010 GeneticVariation BEFREE In the AMI cohort, associations between: DIO1 rs12095080 and hypertension; DIO2 rs225015 and diabetes mellitus; and the OATP1C1 rs974453 genotype, and AMI type were established. 29641285 2018
dbSNP: rs974453
rs974453
Entrez Id: 53919
Gene Symbol: SLCO1C1
SLCO1C1
CUI: C0155626
Disease:
Acute myocardial infarction
0.010 GeneticVariation BEFREE In the AMI cohort, associations between: DIO1 rs12095080 and hypertension; DIO2 rs225015 and diabetes mellitus; and the OATP1C1 rs974453 genotype, and AMI type were established. 29641285 2018
dbSNP: rs3794271
rs3794271
Entrez Id: 53919
Gene Symbol: SLCO1C1
SLCO1C1
CUI: C0003873
Disease:
Rheumatoid Arthritis
0.010 GeneticVariation BEFREE Importantly, the allele that was previously associated with the lack of response to rheumatoid arthritis (G allele, single-nucleotide polymorphism rs3794271) was associated with a higher anti-TNF efficacy in psoriasis. 25403996 2015
dbSNP: rs3794271
rs3794271
Entrez Id: 53919
Gene Symbol: SLCO1C1
SLCO1C1
CUI: C0033860
Disease:
Psoriasis
0.010 GeneticVariation BEFREE Importantly, the allele that was previously associated with the lack of response to rheumatoid arthritis (G allele, single-nucleotide polymorphism rs3794271) was associated with a higher anti-TNF efficacy in psoriasis. 25403996 2015
dbSNP: rs36010656
rs36010656
Entrez Id: 53919
Gene Symbol: SLCO1C1
SLCO1C1
CUI: C0011581
Disease:
Depressive disorder
0.010 GeneticVariation BEFREE Both the OATP1C1-intron3C > T and the OATP1C1-C3035T polymorphism, but not the OATP1C1-Pro143Thr polymorphism, were associated with symptoms of fatigue and depression. 18410547 2008
dbSNP: rs36010656
rs36010656
Entrez Id: 53919
Gene Symbol: SLCO1C1
SLCO1C1
CUI: C0344315
Disease:
Depressed mood
0.010 GeneticVariation BEFREE Both the OATP1C1-intron3C > T and the OATP1C1-C3035T polymorphism, but not the OATP1C1-Pro143Thr polymorphism, were associated with symptoms of fatigue and depression. 18410547 2008
dbSNP: rs36010656
rs36010656
Entrez Id: 53919
Gene Symbol: SLCO1C1
SLCO1C1
CUI: C0011570
Disease:
Mental Depression
0.010 GeneticVariation BEFREE Both the OATP1C1-intron3C > T and the OATP1C1-C3035T polymorphism, but not the OATP1C1-Pro143Thr polymorphism, were associated with symptoms of fatigue and depression. 18410547 2008
dbSNP: rs36010656
rs36010656
Entrez Id: 53919
Gene Symbol: SLCO1C1
SLCO1C1
CUI: C0015672
Disease:
Fatigue
0.010 GeneticVariation BEFREE Both the OATP1C1-intron3C > T and the OATP1C1-C3035T polymorphism, but not the OATP1C1-Pro143Thr polymorphism, were associated with symptoms of fatigue and depression. 18410547 2008