rs7665090, MANBA

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.
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 0.800 1.000 2 2011 2012
Biliary cirrhosis
CUI: C0023892
Disease: Biliary cirrhosis
36 0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 0.700 1.000 1 2011 2011
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 0.700 1.000 1 2013 2013
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 0.700 1.000 1 2015 2015
CREST Syndrome
CUI: C0206138
Disease: CREST Syndrome
6 0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 0.010 1.000 1 2015 2015
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 0.010 1.000 1 2015 2015