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: rs1398859175
rs1398859175
1 1.000 0.160 12 112477882 missense variant A/G snv 7.0E-06 0.700 0
dbSNP: rs1553353452
rs1553353452
1 1.000 0.160 2 39007033 missense variant C/T snv 0.700 0
dbSNP: rs397507477
rs397507477
2 1.000 0.160 7 140777995 missense variant G/A snv 0.700 0
dbSNP: rs397507518
rs397507518
2 0.925 0.160 12 112450508 missense variant G/A snv 0.700 0
dbSNP: rs397509343
rs397509343
1 1.000 0.160 7 140801531 missense variant A/C snv 0.700 0
dbSNP: rs397516822
rs397516822
1 1.000 0.160 3 12608823 missense variant T/C snv 0.700 0
dbSNP: rs397516825
rs397516825
1 1.000 0.160 3 12604204 missense variant T/C snv 0.700 0
dbSNP: rs397516891
rs397516891
1 1.000 0.160 7 140781599 missense variant G/C snv 0.700 0
dbSNP: rs397516903
rs397516903
2 0.925 0.200 7 140801533 missense variant A/C;G snv 0.700 0
dbSNP: rs397516904
rs397516904
2 0.925 0.200 7 140801487 missense variant T/C;G snv 0.700 0
dbSNP: rs397516905
rs397516905
1 1.000 0.160 7 140801479 missense variant C/G snv 0.700 0
dbSNP: rs397517163
rs397517163
1 1.000 0.160 2 38996981 missense variant A/G snv 0.700 0
dbSNP: rs397517166
rs397517166
2 0.925 0.160 2 39058683 missense variant G/C snv 0.700 0
dbSNP: rs397517174
rs397517174
3 0.925 0.160 2 39054822 missense variant A/C;G snv 0.700 0
dbSNP: rs587782971
rs587782971
1 1.000 0.160 3 12608895 missense variant A/G snv 0.700 0
dbSNP: rs587782972
rs587782972
1 1.000 0.160 3 12591729 missense variant C/A snv 0.700 0
dbSNP: rs727502904
rs727502904
2 0.925 0.200 7 140734763 missense variant G/A;T snv 0.700 0
dbSNP: rs727503384
rs727503384
1 1.000 0.160 3 12611985 missense variant G/C snv 0.700 0
dbSNP: rs727504375
rs727504375
2 0.925 0.200 7 140778059 missense variant T/G snv 0.700 0
dbSNP: rs727504382
rs727504382
2 0.925 0.200 19 4101105 missense variant C/T snv 0.700 0
dbSNP: rs730881003
rs730881003
1 1.000 0.160 3 12585794 missense variant A/G snv 0.700 0
dbSNP: rs730881014
rs730881014
15 0.776 0.360 1 155904494 stop gained A/C;G;T snv 0.700 0
dbSNP: rs869025190
rs869025190
1 1.000 0.160 1 155910462 missense variant C/A snv 0.700 0
dbSNP: rs869025192
rs869025192
1 1.000 0.160 1 155904499 missense variant C/G snv 0.700 0
dbSNP: rs869025195
rs869025195
11 0.790 0.280 1 155904493 missense variant T/G snv 0.700 0