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: rs121909574
rs121909574
17 0.724 0.400 6 10404509 missense variant T/A;C;G snv 4.6E-06 0.810 1.000 3 2008 2015
dbSNP: rs121909575
rs121909575
1 1.000 0.040 6 10402590 missense variant C/T snv 0.800 1.000 1 2008 2008
dbSNP: rs151344528
rs151344528
1 1.000 0.040 6 10404512 missense variant G/A;C snv 4.5E-06 0.800 1.000 1 2008 2008
dbSNP: rs151344531
rs151344531
2 0.925 0.120 6 10402608 missense variant G/A snv 0.710 1.000 1 2012 2012
dbSNP: rs793888540
rs793888540
9 0.851 0.080 6 10404623 missense variant G/T snv 0.700 1.000 1 2015 2015
dbSNP: rs793888541
rs793888541
7 0.807 0.120 6 10404631 missense variant A/T snv 0.700 1.000 1 2015 2015
dbSNP: rs151344525
rs151344525
3 0.925 0.040 6 10404562 missense variant C/G;T snv 0.700 0
dbSNP: rs151344530
rs151344530
3 0.925 0.040 6 10404511 missense variant C/G;T snv 0.700 0
dbSNP: rs1554110673
rs1554110673
1 1.000 0.040 6 10398417 stop lost T/C snv 0.700 0
dbSNP: rs1554110994
rs1554110994
1 1.000 0.040 6 10400584 missense variant C/G snv 0.700 0
dbSNP: rs1554111717
rs1554111717
1 1.000 0.040 6 10404523 missense variant C/T snv 0.700 0
dbSNP: rs1554111734
rs1554111734
1 1.000 0.040 6 10404559 missense variant A/G snv 0.700 0
dbSNP: rs1554111749
rs1554111749
1 1.000 0.040 6 10404566 missense variant G/A snv 0.700 0
dbSNP: rs1554111751
rs1554111751
1 1.000 0.040 6 10404575 missense variant C/T snv 0.700 0
dbSNP: rs1554112492
rs1554112492
1 1.000 0.040 6 10409973 frameshift variant -/CCGTGCA delins 0.700 0
dbSNP: rs267607108
rs267607108
1 1.000 0.040 6 10400587 missense variant C/T snv 0.700 0