rs9920, CAV1

N. diseases: 3
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.
QT interval feature (observable entity)
CUI: C0429028
Disease: QT interval feature (observable entity)
226 1.000 0.040 7 116560038 3 prime UTR variant T/C snv 6.7E-02 0.700 1.000 1 2014 2014
Reticulocyte count (procedure)
CUI: C0206161
Disease: Reticulocyte count (procedure)
474 1.000 0.040 7 116560038 3 prime UTR variant T/C snv 6.7E-02 0.700 1.000 1 2016 2016
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 1.000 0.040 7 116560038 3 prime UTR variant T/C snv 6.7E-02 0.010 1.000 1 2012 2012