rs587776820, 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 7142871 frameshift variant GTCCTGGT/- delins 0.700 0