CSF1, colony stimulating factor 1, 1435

N. diseases: 259; N. variants: 7
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: rs333947
rs333947
1 109928142 intron variant G/A snv 0.13
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 2 2016 2019
dbSNP: rs333947
rs333947
1 109928142 intron variant G/A snv 0.13
CUI: C0201973
Disease: Creatine kinase measurement
Creatine kinase measurement
0.700 1.000 1 2018 2018
dbSNP: rs333947
rs333947
1 109928142 intron variant G/A snv 0.13
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs333947
rs333947
1 109928142 intron variant G/A snv 0.13
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs333947
rs333947
1 109928142 intron variant G/A snv 0.13
CUI: C0750880
Disease: Monocyte count result
Monocyte count result
0.700 1.000 1 2016 2016
dbSNP: rs333947
rs333947
1 109928142 intron variant G/A snv 0.13
Aspartate aminotransferase measurement
0.700 1.000 1 2018 2018
dbSNP: rs333947
rs333947
1 109928142 intron variant G/A snv 0.13
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs1058885
rs1058885
0.925 0.080 1 109923844 missense variant T/C snv 0.38 0.39
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis
Stomatognathic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1058885
rs1058885
0.925 0.080 1 109923844 missense variant T/C snv 0.38 0.39
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2050462
rs2050462
0.925 0.120 1 109930334 3 prime UTR variant T/A;G snv
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2050462
rs2050462
0.925 0.120 1 109930334 3 prime UTR variant T/A;G snv
Conventional (Clear Cell) Renal Cell Carcinoma
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2297706
rs2297706
1.000 0.040 1 109914244 intron variant C/A;T snv 0.22 0.25
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis
Stomatognathic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs333951
rs333951
0.925 0.120 1 109909068 upstream gene variant T/C snv 0.74
Conventional (Clear Cell) Renal Cell Carcinoma
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 < 0.001 1 2018 2018
dbSNP: rs333951
rs333951
0.925 0.120 1 109909068 upstream gene variant T/C snv 0.74
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 < 0.001 1 2018 2018
dbSNP: rs333967
rs333967
1.000 0.040 1 109917151 intron variant C/T snv 0.28
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis
Stomatognathic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs777521033
rs777521033
1.000 1 109923705 missense variant G/A;T snv 8.0E-06
CUI: C2363741
Disease: HIV-1 infection
HIV-1 infection
0.010 1.000 1 2006 2006