TNFSF12, TNF superfamily member 12, 8742

N. diseases: 123; 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: rs11078696
rs11078696 		17 7555982 intron variant G/T snv 0.60
CUI: C0523912
Disease: Testosterone measurement
Testosterone measurement 		0.700 1.000 1 2019 2019
dbSNP: rs4511593
rs4511593 		17 7552219 intron variant C/A;G;T snv
CUI: C0005612
Disease: Birth Weight
Birth Weight 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2019 2019
dbSNP: rs62059803
rs62059803 		17 7548527 upstream gene variant C/T snv 0.15
CUI: C0523912
Disease: Testosterone measurement
Testosterone measurement 		0.700 1.000 1 2019 2019
dbSNP: rs78744936
rs78744936 		17 7558026 non coding transcript exon variant G/A snv 0.19
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs80067372
rs80067372 		17 7549435 non coding transcript exon variant G/A;C snv 0.18; 1.9E-05
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs9899183
rs9899183 		1.000 0.080 17 7549660 intron variant C/G;T snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs9899183
rs9899183 		1.000 0.080 17 7549660 intron variant C/G;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs9899183
rs9899183 		1.000 0.080 17 7549660 intron variant C/G;T snv
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs1421612208
rs1421612208 		1.000 0.040 17 7556804 missense variant G/A snv
CUI: C0022739
Disease: Klippel-Trenaunay-Weber Syndrome
Klippel-Trenaunay-Weber Syndrome 		Cardiovascular Diseases 0.010 1.000 1 2004 2004