Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12631066
rs12631066
Entrez Id: 10015
Gene Symbol: PDCD6IP
PDCD6IP
CUI: C0205682
Disease:
Waist-Hip Ratio
C 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs12631066
rs12631066
Entrez Id: 10015
Gene Symbol: PDCD6IP
PDCD6IP
CUI: C0205682
Disease:
Waist-Hip Ratio
C 0.700 GeneticVariation GWASCAT Association of Genetic Variants Related to Gluteofemoral vs Abdominal Fat Distribution With Type 2 Diabetes, Coronary Disease, and Cardiovascular Risk Factors. 30575882 2018
dbSNP: rs28381975
rs28381975
Entrez Id: 10015;105377023
Gene Symbol: PDCD6IP;LOC105377023
PDCD6IP;LOC105377023
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE The aim of this case-control study is to investigate the relationship between the PDCD6IP 15 bp insertion/deletion (I/D) polymorphism (rs28381975) and BC risk in an Iranian population. 26063962 2015
dbSNP: rs28381975
rs28381975
Entrez Id: 10015;105377023
Gene Symbol: PDCD6IP;LOC105377023
PDCD6IP;LOC105377023
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE The aim of this case-control study is to investigate the relationship between the PDCD6IP 15 bp insertion/deletion (I/D) polymorphism (rs28381975) and BC risk in an Iranian population. 26063962 2015
dbSNP: rs28381975
rs28381975
Entrez Id: 10015;105377023
Gene Symbol: PDCD6IP;LOC105377023
PDCD6IP;LOC105377023
CUI: C0007131
Disease:
Non-Small Cell Lung Carcinoma
0.010 GeneticVariation BEFREE The aim of this study is to investigate the relationship between PDCD6IP insertion/deletion (I/D) polymorphism (rs28381975) and NSCLC risk in a Chinese population. 24870593 2014
dbSNP: rs28381975
rs28381975
Entrez Id: 10015;105377023
Gene Symbol: PDCD6IP;LOC105377023
PDCD6IP;LOC105377023
CUI: C0019163
Disease:
Hepatitis B
0.010 GeneticVariation BEFREE Moreover, significant differences were observed within HCC patients concerning genotypic frequencies of rs28381975 after stratifying by tumor stages and HBV infection. 23777424 2013
dbSNP: rs28381975
rs28381975
Entrez Id: 10015;105377023
Gene Symbol: PDCD6IP;LOC105377023
PDCD6IP;LOC105377023
CUI: C2239176
Disease:
Liver carcinoma
0.010 GeneticVariation BEFREE By analyzing 390 HCC cases and 431 healthy controls in a Chinese population, we used a candidate gene approach to evaluate the association between a 15-bp insertion/deletion (indel) polymorphism (rs28381975) in the promoter region of the programmed cell death 6 interacting protein (PDCD6IP) gene and HCC susceptibility. 23777424 2013