Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1329693158
rs1329693158
INSR
2 0.925 0.120 19 7184454 missense variant C/T snv 4.0E-06 0.010 1.000 1 1995 1995