PGR, progesterone receptor, 5241

N. diseases: 392; N. variants: 33
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10895054
rs10895054
0.925 0.080 11 101039579 intron variant A/T snv 0.11
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2013 2013
dbSNP: rs10895054
rs10895054
0.925 0.080 11 101039579 intron variant A/T snv 0.11
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2013 2013
dbSNP: rs10895068
rs10895068
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02
CUI: C0238033
Disease: Carcinoma of Male Breast
Carcinoma of Male Breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2015 2015
dbSNP: rs10895068
rs10895068
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2016 2016
dbSNP: rs10895068
rs10895068
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02
CUI: C0085083
Disease: Ovarian Hyperstimulation Syndrome
Ovarian Hyperstimulation Syndrome
Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs10895068
rs10895068
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs10895068
rs10895068
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs10895068
rs10895068
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02
CUI: C0014175
Disease: Endometriosis
Endometriosis
Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2011 2011
dbSNP: rs10895068
rs10895068
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs10895068
rs10895068
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02
CUI: C4317171
Disease: Adolescent Obesity
Adolescent Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2016 2016
dbSNP: rs10895068
rs10895068
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs10895068
rs10895068
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2016 2016
dbSNP: rs10895068
rs10895068
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs10895068
rs10895068
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02
CUI: C0242787
Disease: Malignant neoplasm of male breast
Malignant neoplasm of male breast
Neoplasms; Skin and Connective Tissue Diseases; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs11224571
rs11224571
11 101047942 intron variant C/A snv 1.2E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs11224571
rs11224571
11 101047942 intron variant C/A snv 1.2E-02
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs11224571
rs11224571
11 101047942 intron variant C/A snv 1.2E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs11571149
rs11571149
0.925 0.080 11 101127937 missense variant G/T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2007 2007
dbSNP: rs11571149
rs11571149
0.925 0.080 11 101127937 missense variant G/T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2007 2007
dbSNP: rs11571151
rs11571151
11 101127486 missense variant C/G;T snv
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs11571151
rs11571151
11 101127486 missense variant C/G;T snv
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs11571151
rs11571151
11 101127486 missense variant C/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs11571151
rs11571151
11 101127486 missense variant C/G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs11571151
rs11571151
11 101127486 missense variant C/G;T snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs11571151
rs11571151
11 101127486 missense variant C/G;T snv
High density lipoprotein measurement
0.700 1.000 1 2012 2012