MDM4, MDM4 regulator of p53, 4194

N. diseases: 265; N. variants: 9
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: rs10900598
rs10900598
0.882 0.120 1 204556440 3 prime UTR variant G/C;T snv 0.38
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth
Neoplasms; Stomatognathic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs10900598
rs10900598
0.882 0.120 1 204556440 3 prime UTR variant G/C;T snv 0.38
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma
Neoplasms; Stomatognathic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs10900598
rs10900598
0.882 0.120 1 204556440 3 prime UTR variant G/C;T snv 0.38
Squamous cell carcinoma of oropharynx
Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs10900598
rs10900598
0.882 0.120 1 204556440 3 prime UTR variant G/C;T snv 0.38
Squamous cell carcinoma of the head and neck
Neoplasms 0.010 1.000 1 2011 2011
dbSNP: rs116197192
rs116197192
0.925 0.080 1 204538255 missense variant A/G snv 4.4E-04 4.7E-04
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2008 2008
dbSNP: rs116197192
rs116197192
0.925 0.080 1 204538255 missense variant A/G snv 4.4E-04 4.7E-04
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2008 2008
dbSNP: rs1380576
rs1380576
0.763 0.240 1 204519150 intron variant G/C snv 0.57
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1380576
rs1380576
0.763 0.240 1 204519150 intron variant G/C snv 0.57
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma
Neoplasms; Stomatognathic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs1380576
rs1380576
0.763 0.240 1 204519150 intron variant G/C snv 0.57
CUI: C0035335
Disease: Retinoblastoma
Retinoblastoma
Neoplasms; Eye Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1380576
rs1380576
0.763 0.240 1 204519150 intron variant G/C snv 0.57
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2010 2010
dbSNP: rs1380576
rs1380576
0.763 0.240 1 204519150 intron variant G/C snv 0.57
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth
Neoplasms; Stomatognathic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs1380576
rs1380576
0.763 0.240 1 204519150 intron variant G/C snv 0.57
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2010 2010
dbSNP: rs1380576
rs1380576
0.763 0.240 1 204519150 intron variant G/C snv 0.57
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1380576
rs1380576
0.763 0.240 1 204519150 intron variant G/C snv 0.57
Squamous cell carcinoma of the head and neck
Neoplasms 0.010 1.000 1 2011 2011
dbSNP: rs2290854
rs2290854
0.925 0.080 1 204546897 intron variant A/G snv 0.65 0.57
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: rs4245739
rs4245739
0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs4245739
rs4245739
0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06
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: rs4245739
rs4245739
0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06
Squamous cell carcinoma of esophagus
Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs4245739
rs4245739
0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2016 2016
dbSNP: rs4245739
rs4245739
0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06
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: rs4245739
rs4245739
0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06
CUI: C0220605
Disease: Adult Non-Hodgkin Lymphoma
Adult Non-Hodgkin Lymphoma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs4245739
rs4245739
0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06
Squamous cell carcinoma of oropharynx
Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2019 2019
dbSNP: rs4245739
rs4245739
0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs4245739
rs4245739
0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06
CUI: C0220612
Disease: Childhood Non-Hodgkin Lymphoma
Childhood Non-Hodgkin Lymphoma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs4245739
rs4245739
0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
Lymphoma, Non-Hodgkin, Familial
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2014 2014