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: rs104894765
rs104894765
2 0.925 0.160 X 50916132 missense variant A/C;G snv 0.800 1.000 1 2004 2004
dbSNP: rs104894763
rs104894763
2 0.925 0.160 X 50910985 missense variant C/T snv 7.0E-04 5.6E-04 0.700 1.000 5 2006 2010
dbSNP: rs104894766
rs104894766
2 0.925 0.160 X 50911009 missense variant C/T snv 4.1E-04 2.9E-04 0.700 1.000 5 2006 2010
dbSNP: rs104894767
rs104894767
3 0.882 0.160 X 50915966 missense variant G/A;T snv 1.0E-02; 2.3E-04 0.700 1.000 5 2006 2010
dbSNP: rs144392417
rs144392417
1 1.000 0.160 X 50910964 missense variant C/A;T snv 6.3E-05 8.5E-05 0.700 1.000 5 2006 2010
dbSNP: rs371418883
rs371418883
1 1.000 0.160 X 50915841 missense variant G/A snv 3.3E-05 0.700 1.000 5 2006 2010
dbSNP: rs782375794
rs782375794
1 1.000 0.160 X 50916413 missense variant C/T snv 1.7E-05 0.700 1.000 5 2006 2010
dbSNP: rs782379521
rs782379521
1 1.000 0.160 X 50916155 missense variant A/G snv 9.8E-05 2.8E-05 0.700 1.000 5 2006 2010
dbSNP: rs782516193
rs782516193
1 1.000 0.160 X 50916045 missense variant G/A snv 6.5E-05 2.8E-05 0.700 1.000 5 2006 2010
dbSNP: rs114823607
rs114823607
1 1.000 0.160 X 50915871 missense variant T/C snv 3.2E-03 8.1E-03 0.700 0
dbSNP: rs375284458
rs375284458
1 1.000 0.160 X 50916089 missense variant T/C;G snv 4.0E-04; 5.5E-06 0.700 0