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: rs11711040
rs11711040 		1.000 0.040 3 54222532 intron variant A/G snv 9.0E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs13319916
rs13319916 		3 54204031 intron variant A/G snv 0.49
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs139882217
rs139882217 		1.000 0.080 3 54695885 intron variant C/T snv 1.2E-02
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2020 2020
dbSNP: rs1562686
rs1562686 		3 54132293 intron variant C/A;G snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs1868513
rs1868513 		3 54130496 intron variant G/A snv 0.38
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs4485754
rs4485754 		3 54200695 intron variant A/G snv 0.24
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs4955912
rs4955912 		3 54962421 intron variant C/T snv 0.39
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs56247223
rs56247223 		3 54608201 intron variant G/A snv 0.25
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2017 2017
dbSNP: rs6805548
rs6805548 		1.000 0.040 3 54222621 intron variant A/G snv 0.39
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs7623444
rs7623444 		3 54140210 intron variant G/A snv 0.51
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs9853714
rs9853714 		3 55038664 intron variant A/G snv 0.20
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs1303530299
rs1303530299 		1.000 0.040 3 54642201 missense variant A/G snv 4.0E-06
CUI: C0240066
Disease: Iron deficiency
Iron deficiency 		Nutritional and Metabolic Diseases 0.020 1.000 2 2013 2014
dbSNP: rs1375515
rs1375515 		1.000 0.040 3 54442613 intron variant C/T snv 0.58
CUI: C0002871
Disease: Anemia
Anemia 		Hemic and Lymphatic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1868505
rs1868505 		1.000 0.040 3 54387228 intron variant T/C snv 0.86
CUI: C0002871
Disease: Anemia
Anemia 		Hemic and Lymphatic Diseases 0.010 1.000 1 2015 2015