rs11499034, SEL1L

N. diseases: 2
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.
Tonometry
CUI: C0040420
Disease: Tonometry
573 1.000 0.120 14 81506097 missense variant T/C snv 1.1E-02 9.7E-03 0.700 1.000 1 2018 2018
Congenital Hyperinsulinism
CUI: C3888018
Disease: Congenital Hyperinsulinism
27 1.000 0.120 14 81506097 missense variant T/C snv 1.1E-02 9.7E-03 0.010 1.000 1 2004 2004