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: rs1122594
rs1122594
1.000 0.040 4 24913606 intron variant C/T snv 0.11
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs11721701
rs11721701
1.000 0.040 4 24922810 intron variant C/A;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs11943001
rs11943001
1.000 0.040 4 24909322 intron variant T/C snv 0.13
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs13131918
rs13131918
4 24871982 intron variant G/A snv 0.40
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018
dbSNP: rs137945355
rs137945355
1.000 0.080 4 24942593 intron variant T/C;G snv
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs41421648
rs41421648
1.000 0.040 4 24922542 intron variant C/T snv 7.7E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs534951121
rs534951121
4 24873319 intron variant CAGAACAGTATGCACCCA/- delins 2.6E-03
CUI: C0424678
Disease: Lean body mass
Lean body mass
0.700 1.000 1 2017 2017
dbSNP: rs7656118
rs7656118
1.000 0.040 4 24922991 intron variant C/T snv 2.0E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs7680589
rs7680589
1.000 0.040 4 24922875 intron variant T/C;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017