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: rs1458766475
rs1458766475
41 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs1940475
rs1940475
4 1.000 0.040 11 102722517 missense variant T/C;G snv 0.54 0.010 1.000 1 2014 2014
dbSNP: rs5361
rs5361
47 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.010 1.000 1 2005 2005
dbSNP: rs6025
rs6025
F5
43 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1.000 1 2003 2003
dbSNP: rs7805622
rs7805622
2 7 56483270 non coding transcript exon variant A/G;T snv 0.010 1.000 1 2015 2015