rs1042838, PGR

N. diseases: 12
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.
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.742 0.240 11 101062681 missense variant C/A;G snv 0.13; 4.0E-06 0.020 0.500 2 2010 2015
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.742 0.240 11 101062681 missense variant C/A;G snv 0.13; 4.0E-06 0.060 0.667 6 2002 2020
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.742 0.240 11 101062681 missense variant C/A;G snv 0.13; 4.0E-06 0.060 0.667 6 2002 2020
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.742 0.240 11 101062681 missense variant C/A;G snv 0.13; 4.0E-06 0.030 1.000 3 2001 2015
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
315 0.742 0.240 11 101062681 missense variant C/A;G snv 0.13; 4.0E-06 0.030 1.000 3 2001 2015
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.742 0.240 11 101062681 missense variant C/A;G snv 0.13; 4.0E-06 0.030 1.000 3 2001 2015
Cholecystolithiasis
CUI: C0947622
Disease: Cholecystolithiasis
62 0.742 0.240 11 101062681 missense variant C/A;G snv 0.13; 4.0E-06 0.010 1.000 1 2012 2012
Cholelithiasis
CUI: C0008350
Disease: Cholelithiasis
90 0.742 0.240 11 101062681 missense variant C/A;G snv 0.13; 4.0E-06 0.010 1.000 1 2012 2012
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.742 0.240 11 101062681 missense variant C/A;G snv 0.13; 4.0E-06 0.010 1.000 1 2016 2016
Gallbladder Carcinoma
CUI: C0235782
Disease: Gallbladder Carcinoma
75 0.742 0.240 11 101062681 missense variant C/A;G snv 0.13; 4.0E-06 0.010 1.000 1 2012 2012
Malignant neoplasm of endometrium
CUI: C0007103
Disease: Malignant neoplasm of endometrium
197 0.742 0.240 11 101062681 missense variant C/A;G snv 0.13; 4.0E-06 0.010 1.000 1 2016 2016
Tension Headache
CUI: C0033893
Disease: Tension Headache
6 0.742 0.240 11 101062681 missense variant C/A;G snv 0.13; 4.0E-06 0.010 1.000 1 2010 2010