rs3197999, MST1;APEH

N. diseases: 16
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.
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 0.850 1.000 7 2008 2017
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 0.830 1.000 8 2008 2017
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 0.820 1.000 7 2008 2017
Primary sclerosing cholangitis
CUI: C0566602
Disease: Primary sclerosing cholangitis
58 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 0.720 1.000 4 2011 2013
Cholangitis, Sclerosing
CUI: C0008313
Disease: Cholangitis, Sclerosing
276 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 0.700 1.000 4 2011 2017
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 0.700 1.000 1 2016 2016
Asthma
CUI: C0004096
Disease: Asthma
1536 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 0.700 1.000 1 2011 2011
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 0.700 1.000 1 2018 2018
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 0.700 1.000 1 2011 2011
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 0.700 1.000 1 2016 2016
Biliary Tract Cancer
CUI: C0750952
Disease: Biliary Tract Cancer
11 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 0.010 1.000 1 2013 2013
Cholangiocarcinoma
CUI: C0206698
Disease: Cholangiocarcinoma
43 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 0.010 1.000 1 2013 2013
Distal colitis
CUI: C0860168
Disease: Distal colitis
3 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 0.010 1.000 1 2010 2010
Extrahepatic Cholangiocarcinoma
CUI: C3805278
Disease: Extrahepatic Cholangiocarcinoma
3 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 0.010 1.000 1 2013 2013
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 0.010 1.000 1 2013 2013
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 0.010 1.000 1 2013 2013