Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs846910
rs846910
0.882 0.160 1 209701909 intron variant A/G snv 0.95
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.020 1.000 2 2011 2017
dbSNP: rs846910
rs846910
0.882 0.160 1 209701909 intron variant A/G snv 0.95
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 1.000 1 2004 2004
dbSNP: rs846910
rs846910
0.882 0.160 1 209701909 intron variant A/G snv 0.95
CUI: C0852036
Disease: Pregnancy associated hypertension
Pregnancy associated hypertension
0.010 1.000 1 2013 2013
dbSNP: rs846910
rs846910
0.882 0.160 1 209701909 intron variant A/G snv 0.95
CUI: C1392786
Disease: Cognitive changes
Cognitive changes
0.010 1.000 1 2006 2006
dbSNP: rs846910
rs846910
0.882 0.160 1 209701909 intron variant A/G snv 0.95
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.010 1.000 1 2011 2011
dbSNP: rs846910
rs846910
0.882 0.160 1 209701909 intron variant A/G snv 0.95
Diabetes Mellitus, Non-Insulin-Dependent
0.010 1.000 1 2017 2017