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: rs1057519524
rs1057519524
2 0.925 0.040 2 165386837 missense variant T/C snv 0.700 0
dbSNP: rs1057519526
rs1057519526
2 0.925 0.040 2 165344679 missense variant C/T snv 0.700 0
dbSNP: rs1057519527
rs1057519527
2 0.925 0.040 2 165374743 missense variant G/A snv 0.700 0
dbSNP: rs1057519528
rs1057519528
2 0.925 0.040 2 165310376 missense variant G/A snv 0.700 0
dbSNP: rs1553567473
rs1553567473
2 0.925 0.040 2 165309193 missense variant A/G snv 0.700 0
dbSNP: rs387906686
rs387906686
23 0.742 0.320 2 165310413 missense variant C/A;T snv 0.700 0
dbSNP: rs794727444
rs794727444
2 0.925 0.040 2 165389451 missense variant G/A;T snv 0.700 0
dbSNP: rs796053130
rs796053130
2 0.925 0.040 2 165373322 missense variant C/T snv 0.700 0
dbSNP: rs879253767
rs879253767
6 0.882 0.080 2 165313738 frameshift variant T/- delins 0.700 0