Source: BEFREE

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: rs2858060
rs2858060
MIR221 ; MIR222
0.925 0.160 X 45747602 intron variant G/A;C snv
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		0.010 1.000 1 2017 2017
dbSNP: rs2858060
rs2858060
MIR221 ; MIR222
0.925 0.160 X 45747602 intron variant G/A;C snv
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		0.010 1.000 1 2019 2019
dbSNP: rs75246947
rs75246947
MIR221 ; MIR222
X 45746891 intron variant T/A snv
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
Gastrointestinal Stromal Tumors 		0.010 1.000 1 2019 2019