PRC1, protein regulator of cytokinesis 1, 9055

N. diseases: 73; N. variants: 8
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: rs8042680
rs8042680
0.882 0.160 15 90978107 intron variant C/A snv 0.54
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.810 1.000 6 2010 2017
dbSNP: rs2290203
rs2290203
0.882 0.160 15 90968837 3 prime UTR variant G/A snv 0.29
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.720 1.000 3 2014 2017
dbSNP: rs12595025
rs12595025
15 90976901 intron variant C/T snv 0.18
Platelet mean volume determination (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs12910825
rs12910825
1.000 0.080 15 90968030 3 prime UTR variant A/G snv 0.57
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs1867226
rs1867226
15 90980483 non coding transcript exon variant C/A;G snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs2290203
rs2290203
0.882 0.160 15 90968837 3 prime UTR variant G/A snv 0.29
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs77554484
rs77554484
1.000 0.080 15 90965985 upstream gene variant C/A;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs10520699
rs10520699
1.000 0.080 15 90979736 intron variant G/A snv 8.6E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.700 0
dbSNP: rs11852999
rs11852999
1.000 0.080 15 90971530 intron variant C/T snv 0.10
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.700 0
dbSNP: rs2290203
rs2290203
0.882 0.160 15 90968837 3 prime UTR variant G/A snv 0.29
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.020 1.000 2 2014 2016
dbSNP: rs1867226
rs1867226
15 90980483 non coding transcript exon variant C/A;G snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2009 2009
dbSNP: rs8042680
rs8042680
0.882 0.160 15 90978107 intron variant C/A snv 0.54
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2016 2016
dbSNP: rs8042680
rs8042680
0.882 0.160 15 90978107 intron variant C/A snv 0.54
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2016 2016