KLF7, Kruppel like factor 7, 8609

N. diseases: 27; 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: rs7583880
rs7583880
2 207134989 intron variant G/A snv 0.65
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 2 2016 2019
dbSNP: rs1263627
rs1263627
2 207112529 intron variant A/T snv 0.24
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs1263671
rs1263671
2 207131723 intron variant T/C snv 0.17
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs1271272
rs1271272
2 207090753 intron variant G/A;C snv
CUI: C0037369
Disease: Smoking
Smoking
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs17282552
rs17282552
2 207109091 intron variant T/C snv 2.2E-02
CUI: C2697765
Disease: Interleukin 17 Measurement
Interleukin 17 Measurement
0.700 1.000 1 2017 2017
dbSNP: rs768090
rs768090
2 207138855 intron variant A/G;T snv
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.700 1.000 1 2016 2016
dbSNP: rs768090
rs768090
2 207138855 intron variant A/G;T snv
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs2284932
rs2284932
0.925 0.200 2 207147785 intron variant G/A snv 0.33
CUI: C1279945
Disease: Acute interstitial pneumonia
Acute interstitial pneumonia
Respiratory Tract Diseases 0.010 < 0.001 1 2015 2015
dbSNP: rs2284932
rs2284932
0.925 0.200 2 207147785 intron variant G/A snv 0.33
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases 0.010 < 0.001 1 2015 2015
dbSNP: rs2302870
rs2302870
0.925 0.120 2 207088682 intron variant T/C;G snv
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 < 0.001 1 2009 2009
dbSNP: rs2302870
rs2302870
0.925 0.120 2 207088682 intron variant T/C;G snv
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 < 0.001 1 2009 2009
dbSNP: rs7568369
rs7568369
0.925 0.120 2 207166591 intron variant G/T snv 0.38
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2009 2009
dbSNP: rs7568369
rs7568369
0.925 0.120 2 207166591 intron variant G/T snv 0.38
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2009 2009