rs8111699, STK11

N. diseases: 6
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
224 0.851 0.200 19 1209715 intron variant C/G snv 0.53 0.020 0.500 2 2013 2015
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.851 0.200 19 1209715 intron variant C/G snv 0.53 0.010 1 2015 2015
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.851 0.200 19 1209715 intron variant C/G snv 0.53 0.010 1 2015 2015
Hyperandrogenism
CUI: C0206081
Disease: Hyperandrogenism
24 0.851 0.200 19 1209715 intron variant C/G snv 0.53 0.010 1.000 1 2010 2010
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.851 0.200 19 1209715 intron variant C/G snv 0.53 0.010 1.000 1 2019 2019
Precocious pubarche
CUI: C0342541
Disease: Precocious pubarche
11 0.851 0.200 19 1209715 intron variant C/G snv 0.53 0.010 1.000 1 2010 2010