rs886037750, INSR

N. diseases: 1
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.
Rabson-Mendenhall Syndrome
CUI: C0271695
Disease: Rabson-Mendenhall Syndrome
11 1.000 0.160 19 7267603 missense variant C/T snv 0.700 1.000 1 2016 2016