rs1997623, CAV1

N. diseases: 9
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.807 0.160 7 116525306 missense variant A/C;G snv 0.86 0.010 1.000 1 2019 2019
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.807 0.160 7 116525306 missense variant A/C;G snv 0.86 0.010 1.000 1 2013 2013
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.807 0.160 7 116525306 missense variant A/C;G snv 0.86 0.010 1.000 1 2013 2013
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.807 0.160 7 116525306 missense variant A/C;G snv 0.86 0.010 1.000 1 2019 2019
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.807 0.160 7 116525306 missense variant A/C;G snv 0.86 0.010 1.000 1 2013 2013
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.807 0.160 7 116525306 missense variant A/C;G snv 0.86 0.010 1.000 1 2018 2018
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.807 0.160 7 116525306 missense variant A/C;G snv 0.86 0.010 1.000 1 2013 2013
Sarcopenia
CUI: C0872084
Disease: Sarcopenia
10 0.807 0.160 7 116525306 missense variant A/C;G snv 0.86 0.010 1.000 1 2015 2015
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.807 0.160 7 116525306 missense variant A/C;G snv 0.86 0.010 1.000 1 2014 2014