TCF7L1, transcription factor 7 like 1, 83439

N. diseases: 39; 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: rs11904127
rs11904127 		2 85257695 intron variant G/A snv 0.48
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs2043230
rs2043230 		2 85256227 intron variant A/T snv 0.52
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs62162674
rs62162674 		2 85275113 intron variant G/C snv 0.33
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs6547598
rs6547598 		1.000 0.080 2 85219363 intron variant A/G snv 0.26
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.700 1.000 1 2019 2019
dbSNP: rs6547599
rs6547599 		2 85220361 intron variant A/T snv 0.66
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs11547160
rs11547160 		1.000 0.040 2 85309292 missense variant G/A snv 4.2E-02 3.8E-02
CUI: C0029410
Disease: Osteoarthritis of hip
Osteoarthritis of hip 		Musculoskeletal Diseases 0.010 1.000 1 2013 2013