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: rs755522953
rs755522953
1 1.000 0.120 16 2103485 missense variant C/T snv 5.5E-05 2.1E-05 0.700 1.000 20 1996 2009
dbSNP: rs776463508
rs776463508
1 1.000 0.120 16 2097890 missense variant G/A;C;T snv 2.8E-05; 9.7E-05; 4.1E-06 0.700 1.000 20 1996 2009
dbSNP: rs778028644
rs778028644
1 1.000 0.120 16 2109736 missense variant C/T snv 3.3E-05 5.6E-05 0.700 1.000 20 1996 2009
dbSNP: rs781263445
rs781263445
1 1.000 0.120 16 2097971 missense variant G/A snv 4.4E-06 1.4E-05 0.700 1.000 20 1996 2009
dbSNP: rs781492044
rs781492044
1 1.000 0.120 16 2093828 missense variant C/T snv 2.9E-05 3.5E-05 0.700 1.000 20 1996 2009
dbSNP: rs886038369
rs886038369
1 1.000 0.120 16 2135508 missense variant G/A snv 6.3E-04 0.700 1.000 20 1996 2009
dbSNP: rs1033550407
rs1033550407
1 1.000 0.120 16 2111442 missense variant G/A snv 2.1E-05 0.700 0
dbSNP: rs1057516202
rs1057516202
1 1.000 0.120 16 2100027 inframe deletion GCT/- del 0.700 0
dbSNP: rs1057516206
rs1057516206
1 1.000 0.120 16 2111624 stop gained A/T snv 0.700 0
dbSNP: rs1060499699
rs1060499699
1 1.000 0.120 16 2117579 missense variant G/T snv 0.700 0
dbSNP: rs1060499702
rs1060499702
1 1.000 0.120 16 2108743 frameshift variant G/- delins 0.700 0
dbSNP: rs1060499704
rs1060499704
1 1.000 0.120 16 2100396 missense variant C/A snv 0.700 0
dbSNP: rs1060499718
rs1060499718
1 1.000 0.120 16 2090418 frameshift variant CA/- delins 0.700 0
dbSNP: rs1114167366
rs1114167366
1 1.000 0.120 16 2097725 splice donor variant AC/- delins 0.700 0
dbSNP: rs1114167370
rs1114167370
1 1.000 0.120 16 2118296 missense variant A/C snv 0.700 0
dbSNP: rs114251396
rs114251396
1 1.000 0.120 16 2089813 missense variant G/A snv 3.7E-03 3.3E-03 0.700 0
dbSNP: rs115538130
rs115538130
1 1.000 0.120 16 2090179 missense variant G/A;T snv 9.3E-04; 4.2E-06 0.700 0
dbSNP: rs1161298621
rs1161298621
1 1.000 0.120 16 2106475 missense variant G/A snv 7.0E-06 0.700 0
dbSNP: rs1167476946
rs1167476946
1 1.000 0.120 16 2092492 missense variant G/A snv 0.700 0
dbSNP: rs1218054241
rs1218054241
1 1.000 0.120 16 2090776 stop gained C/A;T snv 4.1E-06 0.700 0
dbSNP: rs1266492292
rs1266492292
1 1.000 0.120 16 2113185 missense variant C/G snv 8.4E-06 0.700 0
dbSNP: rs1282205691
rs1282205691
1 1.000 0.120 16 2118717 missense variant C/A;T snv 0.700 0
dbSNP: rs1327414405
rs1327414405
1 1.000 0.120 16 2092500 missense variant C/T snv 4.0E-06 0.700 0
dbSNP: rs1377414968
rs1377414968
1 1.000 0.120 16 2109801 stop gained G/A;C snv 4.1E-06 0.700 0
dbSNP: rs1383930225
rs1383930225
1 1.000 0.120 16 2108919 missense variant G/A snv 7.0E-06 0.700 0