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: rs1057519807
rs1057519807
1 1.000 0.040 19 4110586 missense variant A/T snv 0.710 1.000 2 2014 2014
dbSNP: rs1057519808
rs1057519808
2 1.000 0.040 19 4117543 missense variant T/G snv 0.710 1.000 2 2013 2014
dbSNP: rs1057519806
rs1057519806
3 0.882 0.200 19 4110583 missense variant T/C snv 0.700 1.000 1 2014 2014
dbSNP: rs1057519809
rs1057519809
1 1.000 0.040 19 4117586 missense variant G/A;C snv 4.0E-06 0.700 1.000 1 2014 2014
dbSNP: rs1057519810
rs1057519810
1 1.000 0.040 19 4117619 missense variant C/A;T snv 4.0E-06 0.700 1.000 1 2014 2014