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: rs1011633
rs1011633
1 1.000 0.040 2 99478337 intron variant C/T snv 0.43 0.700 1.000 1 2013 2013
dbSNP: rs1053544
rs1053544
1 1.000 0.040 2 99405808 non coding transcript exon variant G/A snv 0.43 0.700 1.000 1 2013 2013
dbSNP: rs11899745
rs11899745
1 1.000 0.040 2 99447610 intron variant A/G snv 0.45 0.700 1.000 1 2013 2013
dbSNP: rs2290261
rs2290261
1 1.000 0.040 2 99404721 intron variant A/G snv 0.43 0.42 0.700 1.000 1 2013 2013
dbSNP: rs3792137
rs3792137
1 1.000 0.040 2 99445286 intron variant C/A snv 0.43 0.700 1.000 1 2013 2013
dbSNP: rs4851206
rs4851206
1 1.000 0.040 2 99451607 intron variant T/A;C;G snv 0.700 1.000 1 2013 2013
dbSNP: rs717454
rs717454
2 1.000 0.040 2 99406310 non coding transcript exon variant T/C;G snv 0.44; 8.2E-06 0.700 1.000 1 2013 2013
dbSNP: rs7585019
rs7585019
1 1.000 0.040 2 99460865 intron variant G/A;C;T snv 0.700 1.000 1 2013 2013
dbSNP: rs769105
rs769105
1 1.000 0.040 2 99461504 intron variant G/A snv 0.43 0.700 1.000 1 2013 2013