MSMB, microseminoprotein beta, 4477

N. diseases: 195; N. variants: 5
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: rs10993994
rs10993994
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 0.800 1.000 37 2008 2020
dbSNP: rs10993994
rs10993994
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.800 1.000 30 2008 2019
dbSNP: rs10993994
rs10993994
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54
Prostate specific antigen measurement
0.800 1.000 3 2010 2017
dbSNP: rs10993994
rs10993994
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs10993994
rs10993994
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2010 2010
dbSNP: rs10993994
rs10993994
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54
CUI: C0013595
Disease: Eczema
Eczema
Skin and Connective Tissue Diseases 0.700 1.000 1 2019 2019
dbSNP: rs61847070
rs61847070
10 46047367 intron variant A/G snv 5.5E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs10993994
rs10993994
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54
CUI: C2677821
Disease: Prostate Cancer, Hereditary, 13
Prostate Cancer, Hereditary, 13
Neoplasms; Male Urogenital Diseases 0.700 0
dbSNP: rs10993994
rs10993994
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.020 1.000 2 2009 2013
dbSNP: rs10993994
rs10993994
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54
Metastasis from malignant tumor of prostate
0.010 1.000 1 2011 2011
dbSNP: rs10993994
rs10993994
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 1.000 1 2009 2009
dbSNP: rs10993994
rs10993994
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs10993994
rs10993994
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54
CUI: C0936223
Disease: Metastatic Prostate Carcinoma
Metastatic Prostate Carcinoma
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2011 2011
dbSNP: rs10993994
rs10993994
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
0.010 1.000 1 2009 2009
dbSNP: rs10993994
rs10993994
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.010 1.000 1 2009 2009
dbSNP: rs10993994
rs10993994
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54
CUI: C0036916
Disease: Sexually Transmitted Diseases
Sexually Transmitted Diseases
Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1802771
rs1802771
0.925 0.080 10 46033507 missense variant A/G;T snv
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis
Nutritional and Metabolic Diseases; Nervous System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1802771
rs1802771
0.925 0.080 10 46033507 missense variant A/G;T snv
Amyotrophic Lateral Sclerosis, Familial
Nutritional and Metabolic Diseases; Nervous System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1804469
rs1804469
0.925 0.120 10 46033495 missense variant T/C snv
CUI: C0236642
Disease: Pick Disease of the Brain
Pick Disease of the Brain
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2013 2013
dbSNP: rs1804469
rs1804469
0.925 0.120 10 46033495 missense variant T/C snv
CUI: C0338451
Disease: Frontotemporal dementia
Frontotemporal dementia
Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders 0.010 1.000 1 2013 2013
dbSNP: rs7904463
rs7904463
0.925 0.080 10 46036353 intron variant G/A snv 0.43
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2011 2011
dbSNP: rs7904463
rs7904463
0.925 0.080 10 46036353 intron variant G/A snv 0.43
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2011 2011