KLB, klotho beta, 152831

N. diseases: 53; N. variants: 6
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: rs11940694
rs11940694 		4 39413373 intron variant A/G snv 0.57
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement 		0.700 1.000 1 2019 2019
dbSNP: rs11940694
rs11940694 		4 39413373 intron variant A/G snv 0.57
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2017 2017
dbSNP: rs11940694
rs11940694 		4 39413373 intron variant A/G snv 0.57
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs1054506960
rs1054506960 		1.000 4 39434549 missense variant G/A snv
CUI: C1262211
Disease: Diarrhoea predominant irritable bowel syndrome
Diarrhoea predominant irritable bowel syndrome 		0.010 1.000 1 2011 2011
dbSNP: rs12152703
rs12152703 		0.925 0.120 4 39420199 intron variant G/T snv 0.28
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2019 2019
dbSNP: rs12152703
rs12152703 		0.925 0.120 4 39420199 intron variant G/T snv 0.28
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		Digestive System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs17618244
rs17618244 		0.925 0.040 4 39446909 missense variant G/A snv 0.18 0.16
CUI: C1262211
Disease: Diarrhoea predominant irritable bowel syndrome
Diarrhoea predominant irritable bowel syndrome 		0.010 1.000 1 2011 2011
dbSNP: rs17618244
rs17618244 		0.925 0.040 4 39446909 missense variant G/A snv 0.18 0.16
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		Digestive System Diseases 0.010 1.000 1 2020 2020
dbSNP: rs7670903
rs7670903 		1.000 0.080 4 39441340 intron variant A/G snv 0.58
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2019 2019
dbSNP: rs7674434
rs7674434 		0.925 0.120 4 39417789 intron variant T/G snv 0.32
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		Digestive System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs7674434
rs7674434 		0.925 0.120 4 39417789 intron variant T/G snv 0.32
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2019 2019