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: rs11075747
rs11075747 		16 69906458 intron variant G/A snv 0.47
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs12926791
rs12926791 		16 69815643 intron variant C/A;G;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs148604553
rs148604553 		16 69795259 intron variant -/CA ins
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs151186597
rs151186597 		16 69878064 intron variant T/C snv 4.3E-02
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs2173714
rs2173714 		16 69844631 intron variant C/G snv 0.39
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs2173714
rs2173714 		16 69844631 intron variant C/G snv 0.39
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs2937124
rs2937124 		16 69828206 intron variant C/T snv 0.28
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs34195470
rs34195470 		1.000 0.040 16 69921787 intron variant A/G snv 0.46
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs3790076
rs3790076 		16 69873542 intron variant G/T snv 0.63
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs4146819
rs4146819 		16 69889660 intron variant C/A snv 0.64
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs4985445
rs4985445 		16 69833932 intron variant A/G snv 0.53
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs56117028
rs56117028 		16 69851026 intron variant T/A snv 1.2E-03
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2015 2015
dbSNP: rs56140069
rs56140069 		16 69761420 upstream gene variant A/T snv 0.12
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs62050038
rs62050038 		16 69768962 intron variant A/T snv 0.12
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs62051384
rs62051384 		0.925 0.120 16 69825279 intron variant C/T snv 0.38
CUI: C0149756
Disease: Fasciitis, Plantar
Fasciitis, Plantar 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs62051384
rs62051384 		0.925 0.120 16 69825279 intron variant C/T snv 0.38
CUI: C0158360
Disease: Fibromatosis, Plantar
Fibromatosis, Plantar 		Neoplasms; Skin and Connective Tissue Diseases; Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs6499255
rs6499255 		16 69796425 intron variant A/G snv 0.34
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs77870048
rs77870048 		16 69931118 intron variant C/T snv 3.1E-02 3.0E-02
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2019 2019
dbSNP: rs77870048
rs77870048 		16 69931118 intron variant C/T snv 3.1E-02 3.0E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs8047194
rs8047194 		16 69857607 intron variant G/T snv 0.52
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2019 2019
dbSNP: rs8047194
rs8047194 		16 69857607 intron variant G/T snv 0.52
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs8057620
rs8057620 		16 69850716 intron variant A/T snv 0.54
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution 		0.700 1.000 1 2019 2019
dbSNP: rs7205289
rs7205289 		0.882 0.200 16 69933102 non coding transcript exon variant C/A snv
CUI: C2981150
Disease: Uranostaphyloschisis
Uranostaphyloschisis 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2011 2011
dbSNP: rs7205289
rs7205289 		0.882 0.200 16 69933102 non coding transcript exon variant C/A snv
CUI: C1837218
Disease: Cleft palate, isolated
Cleft palate, isolated 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases 0.010 1.000 1 2011 2011
dbSNP: rs7205289
rs7205289 		0.882 0.200 16 69933102 non coding transcript exon variant C/A snv
CUI: C0008925
Disease: Cleft Palate
Cleft Palate 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases 0.010 1.000 1 2011 2011