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: rs1057519806
rs1057519806
3 0.882 0.200 19 4110583 missense variant T/C snv 0.710 1.000 1 2015 2015
dbSNP: rs727504370
rs727504370
2 0.925 0.200 19 4110558 missense variant T/C snv 0.700 1.000 4 2007 2018
dbSNP: rs121434497
rs121434497
2 0.925 0.160 19 4117552 missense variant A/C;T snv 0.700 1.000 1 2006 2006
dbSNP: rs121434498
rs121434498
6 0.807 0.280 19 4117553 missense variant A/C;G;T snv 0.700 1.000 1 2008 2008
dbSNP: rs121434499
rs121434499
2 0.925 0.160 19 4110559 missense variant A/G snv 0.700 1.000 1 2008 2008
dbSNP: rs267607230
rs267607230
2 0.925 0.160 19 4110576 missense variant G/A;C;T snv 0.700 1.000 1 2010 2010
dbSNP: rs727504382
rs727504382
2 0.925 0.200 19 4101105 missense variant C/T snv 0.700 0
dbSNP: rs730880517
rs730880517
1 1.000 0.160 19 4117541 missense variant T/C snv 0.700 0