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: rs111033624
rs111033624
1 1.000 0.080 X 124346737 missense variant G/C snv 0.700 1.000 11 1998 2006
dbSNP: rs111033626
rs111033626
1 1.000 0.080 X 124370276 missense variant C/T snv 0.700 1.000 11 1998 2006
dbSNP: rs111033627
rs111033627
1 1.000 0.080 X 124370177 missense variant C/T snv 0.700 1.000 11 1998 2006
dbSNP: rs111033630
rs111033630
1 1.000 0.080 X 124365787 stop gained G/T snv 0.700 1.000 11 1998 2006