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: rs888801
rs888801
1.000 0.040 5 102755940 intron variant A/G snv 2.7E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs13175330
rs13175330
5 102840757 intron variant A/G snv 7.8E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs375869205
rs375869205
1.000 0.080 5 103003097 missense variant C/G;T snv
Familial Alzheimer's disease of early onset
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2010 2010