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: rs1040026
rs1040026 		1.000 0.080 12 70816898 intron variant T/C snv 4.3E-02
CUI: C2076600
Disease: Influenza due to Influenza A virus subtype H1N1
Influenza due to Influenza A virus subtype H1N1 		Infections; Respiratory Tract Diseases 0.700 1.000 1 2015 2015
dbSNP: rs11178393
rs11178393 		1.000 12 70756878 intron variant T/C snv 8.8E-02
CUI: C2242776
Disease: Plexiform leiomyoma
Plexiform leiomyoma 		0.700 1.000 1 2019 2019
dbSNP: rs11178393
rs11178393 		1.000 12 70756878 intron variant T/C snv 8.8E-02
CUI: C0042133
Disease: Uterine Fibroids
Uterine Fibroids 		Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs12229663
rs12229663 		1.000 12 70856216 intron variant A/G;T snv
CUI: C0034951
Disease: Refractive Errors
Refractive Errors 		Eye Diseases 0.700 1.000 1 2013 2013
dbSNP: rs12229663
rs12229663 		1.000 12 70856216 intron variant A/G;T snv
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction 		0.700 1.000 1 2013 2013
dbSNP: rs12813125
rs12813125 		12 70729668 intron variant C/T snv 6.8E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs12824973
rs12824973 		12 70706667 intron variant G/A snv 6.8E-02
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs1513105
rs1513105 		1.000 0.040 12 70704388 intron variant T/G snv 0.47
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs3803036
rs3803036 		1.000 0.040 12 70745884 missense variant T/A;C snv 0.77
CUI: C0271183
Disease: Severe myopia
Severe myopia 		Eye Diseases 0.010 1.000 1 2013 2013