Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61764370
rs61764370
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.020 GeneticVariation BEFREE Results demonstrated that TT genotype and T allele of rs712 were associated with the increased risk of CRC; the patients with GG genotype and G allele of rs61764370 had a shorter survival and a higher risk of relapse or metastasis of CRC. 26515332

2016

dbSNP: rs61764370
rs61764370
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.020 GeneticVariation BEFREE The objective of the present study was to explore the molecular mechanism with which a single nucleotide polymorphism (rs61764370) interferes with the interaction between the 3'-untranslated region (3'-UTR) of Kirsten rat sarcoma viral oncogene homolog (KRAS) and let-7a, and its association with the metastasis of osteosarcoma (OS). 27430246

2016

dbSNP: rs61764370
rs61764370
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.020 GeneticVariation BEFREE We have reported the analysis performed on the role of the polymorphism located in the KRAS-LCS (rs61764370) which is involved in the disruption of the let-7 complementary site in NSCLC patients enrolled within the TAILOR trial, a randomised trial comparing erlotinib versus docetaxel in second line treatment. 26573509

2015

dbSNP: rs61764370
rs61764370
Squamous cell carcinoma of the head and neck
0.020 GeneticVariation BEFREE The TG/GG rs61764370 KRAS-variant is a potential predictive biomarker for poor platinum response in R/M HNSCC patients. 25081901

2014

dbSNP: rs61764370
rs61764370
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.020 GeneticVariation BEFREE KRAS rs61764370 is associated with HER2-overexpressed and poorly-differentiated breast cancer in hormone replacement therapy users: a case control study. 22436609

2012

dbSNP: rs61764370
rs61764370
CUI: C0014175
Disease: Endometriosis
Endometriosis
0.020 GeneticVariation BEFREE Our results do not support the suggestion that carrying the minor allele at rs61764370 contributes to a significant number of endometriosis cases and rs61764370 is, therefore, unlikely to be a useful marker of endometriosis risk. 23010532

2012

dbSNP: rs61764370
rs61764370
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.020 GeneticVariation BEFREE KRAS rs61764370 is associated with HER2-overexpressed and poorly-differentiated breast cancer in hormone replacement therapy users: a case control study. 22436609

2012

dbSNP: rs61764370
rs61764370
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.020 GeneticVariation BEFREE Recently, a variant allele in the 3'UTR of the KRAS gene (rs61764370 T>G) was shown to be associated with an increased risk for developing non-small cell lung cancer, as well as ovarian cancer, and was most enriched in ovarian cancer patients from hereditary breast and ovarian cancer families. 20676756

2011

dbSNP: rs61764370
rs61764370
Stage III Gallbladder Cancer AJCC v8
0.010 GeneticVariation BEFREE To address this research question, we evaluated whether rs61764370 variant is associated with gallbladder cancer susceptibility and clinical outcomes. 27620744

2016

dbSNP: rs61764370
rs61764370
CUI: C0235782
Disease: Gallbladder Carcinoma
Gallbladder Carcinoma
0.010 GeneticVariation BEFREE To address this research question, we evaluated whether rs61764370 variant is associated with gallbladder cancer susceptibility and clinical outcomes. 27620744

2016

dbSNP: rs61764370
rs61764370
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
Myeloid Leukemia, Chronic
0.010 GeneticVariation BEFREE To the best of our knowledge, this study is the first to show a significant association of the KRAS_rs61764370 SNP with CML. 27221928

2016

dbSNP: rs61764370
rs61764370
Stage IIA Gallbladder Cancer AJCC v8
0.010 GeneticVariation BEFREE To address this research question, we evaluated whether rs61764370 variant is associated with gallbladder cancer susceptibility and clinical outcomes. 27620744

2016

dbSNP: rs61764370
rs61764370
CUI: C4525297
Disease: Stage 0 Gallbladder Cancer AJCC v8
Stage 0 Gallbladder Cancer AJCC v8
0.010 GeneticVariation BEFREE To address this research question, we evaluated whether rs61764370 variant is associated with gallbladder cancer susceptibility and clinical outcomes. 27620744

2016

dbSNP: rs61764370
rs61764370
Stage IIB Gallbladder Cancer AJCC v8
0.010 GeneticVariation BEFREE To address this research question, we evaluated whether rs61764370 variant is associated with gallbladder cancer susceptibility and clinical outcomes. 27620744

2016

dbSNP: rs61764370
rs61764370
CUI: C1261473
Disease: Sarcoma
Sarcoma
0.010 GeneticVariation BEFREE The objective of the present study was to explore the molecular mechanism with which a single nucleotide polymorphism (rs61764370) interferes with the interaction between the 3'-untranslated region (3'-UTR) of Kirsten rat sarcoma viral oncogene homolog (KRAS) and let-7a, and its association with the metastasis of osteosarcoma (OS). 27430246

2016

dbSNP: rs61764370
rs61764370
CUI: C1167791
Disease: Skin toxicity
Skin toxicity
0.010 GeneticVariation BEFREE This pilot study provides preliminary evidence supporting genetic variation of EGFR (rs2227983), KRAS (rs61764370) and FCGR2A (rs180127) as useful biomarkers for predicting reduced skin toxicity in HNSCC patients treated with a cetuximab-based therapy. 27938998

2016

dbSNP: rs61764370
rs61764370
CUI: C4525305
Disease: Stage IV Gallbladder Cancer AJCC v8
Stage IV Gallbladder Cancer AJCC v8
0.010 GeneticVariation BEFREE To address this research question, we evaluated whether rs61764370 variant is associated with gallbladder cancer susceptibility and clinical outcomes. 27620744

2016

dbSNP: rs61764370
rs61764370
CUI: C0153452
Disease: Malignant neoplasm of gallbladder
Malignant neoplasm of gallbladder
0.010 GeneticVariation BEFREE To address this research question, we evaluated whether rs61764370 variant is associated with gallbladder cancer susceptibility and clinical outcomes. 27620744

2016

dbSNP: rs61764370
rs61764370
CUI: C4551686
Disease: Malignant neoplasm of soft tissue
Malignant neoplasm of soft tissue
0.010 GeneticVariation BEFREE The objective of the present study was to explore the molecular mechanism with which a single nucleotide polymorphism (rs61764370) interferes with the interaction between the 3'-untranslated region (3'-UTR) of Kirsten rat sarcoma viral oncogene homolog (KRAS) and let-7a, and its association with the metastasis of osteosarcoma (OS). 27430246

2016

dbSNP: rs61764370
rs61764370
CUI: C0151908
Disease: Dry skin
Dry skin
0.010 GeneticVariation BEFREE A significant association with dry skin and global cetuximab-related toxicity was observed for the KRAS-LCS6 (rs61764370) variant (p<0.05); carriers of the G allele (genotypes TG+GG) in the dominant model were observed to have a decreased susceptibility of developing dry skin (OR=0.287 [95%CI=0.119-0.695]). 27938998

2016

dbSNP: rs61764370
rs61764370
Malignant neoplasm of colon and/or rectum
0.010 GeneticVariation BEFREE A PubMed search was conducted to identify all studies reporting on KRAS let-7 microRNA-binding site polymorphism (LCS6; rs61764370) and colorectal cancer outcome. 24890702

2014

dbSNP: rs61764370
rs61764370
Secondary malignant neoplasm of colon and/or rectum
0.010 GeneticVariation BEFREE Recent studies have reported associations between a variant allele in a let-7 microRNA complementary site (LCS6) within the 3'untranslated region (3'UTR) of KRAS (rs61764370) and clinical outcome in metastatic colorectal cancer (mCRC) patients receiving cetuximab. 23167843

2012

dbSNP: rs61764370
rs61764370
CUI: C0346153
Disease: Breast Cancer, Familial
Breast Cancer, Familial
0.010 GeneticVariation BEFREE Our data do not support the hypothesis that the KRAS variant rs61764370 is implicated in the aetiology of sporadic or of familial breast cancer. 22436609

2012

dbSNP: rs61764370
rs61764370
Hereditary Breast and Ovarian Cancer Syndrome
0.010 GeneticVariation BEFREE Recently, a variant allele in the 3'UTR of the KRAS gene (rs61764370 T>G) was shown to be associated with an increased risk for developing non-small cell lung cancer, as well as ovarian cancer, and was most enriched in ovarian cancer patients from hereditary breast and ovarian cancer families. 20676756

2011

dbSNP: rs61764370
rs61764370
CUI: C0677886
Disease: Epithelial ovarian cancer
Epithelial ovarian cancer
0.010 GeneticVariation BEFREE The role of KRAS rs61764370 in invasive epithelial ovarian cancer: implications for clinical testing. 21385923

2011