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: rs1114167494
rs1114167494
3 1.000 0.120 11 64808031 missense variant C/A snv 0.010 1.000 1 1999 1999
dbSNP: rs1157581823
rs1157581823
1 11 64810060 missense variant T/C snv 7.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs607969
rs607969
2 1.000 0.080 11 64808033 missense variant C/T snv 1.2E-02 1.3E-02 0.010 1.000 1 2004 2004
dbSNP: rs886039413
rs886039413
1 11 64809818 stop gained G/A snv 0.010 1.000 1 1999 1999