rs1799801, ERCC4

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.
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.807 0.360 16 13948101 synonymous variant T/C snv 0.27 0.25 0.010 1.000 1 2016 2016
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.807 0.360 16 13948101 synonymous variant T/C snv 0.27 0.25 0.010 1 2013 2013
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.807 0.360 16 13948101 synonymous variant T/C snv 0.27 0.25 0.010 1.000 1 2012 2012
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.807 0.360 16 13948101 synonymous variant T/C snv 0.27 0.25 0.010 1.000 1 2012 2012
Squamous cell carcinoma of oropharynx
33 0.807 0.360 16 13948101 synonymous variant T/C snv 0.27 0.25 0.010 1.000 1 2005 2005
Squamous cell carcinoma of the head and neck
348 0.807 0.360 16 13948101 synonymous variant T/C snv 0.27 0.25 0.010 1.000 1 2017 2017
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.807 0.360 16 13948101 synonymous variant T/C snv 0.27 0.25 0.010 1 2013 2013
Vomiting
CUI: C0042963
Disease: Vomiting
23 0.807 0.360 16 13948101 synonymous variant T/C snv 0.27 0.25 0.010 1.000 1 2017 2017
Xeroderma pigmentosum, group F
CUI: C0268140
Disease: Xeroderma pigmentosum, group F
31 0.807 0.360 16 13948101 synonymous variant T/C snv 0.27 0.25 0.010 1.000 1 2016 2016