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: rs10842750
rs10842750
2 0.925 0.120 12 26537632 intron variant A/C;T snv 0.710 1.000 1 2015 2015
dbSNP: rs1002835
rs1002835
1 1.000 0.040 12 26539294 intron variant T/A snv 0.57 0.010 1.000 1 2015 2015
dbSNP: rs11048526
rs11048526
1 1.000 0.040 12 26449331 intron variant G/A snv 2.7E-02 0.010 1.000 1 2019 2019
dbSNP: rs11048570
rs11048570
1 1.000 0.040 12 26539754 intron variant G/A snv 0.57 0.010 1.000 1 2015 2015
dbSNP: rs11048572
rs11048572
1 1.000 0.040 12 26540242 intron variant T/A;C snv 0.010 1.000 1 2015 2015
dbSNP: rs1531928
rs1531928
1 1.000 0.040 12 26538266 intron variant A/G snv 0.57 0.010 1.000 1 2015 2015
dbSNP: rs16931011
rs16931011
1 1.000 0.040 12 26575582 intron variant A/G snv 0.20 0.010 1.000 1 2015 2015
dbSNP: rs2017510
rs2017510
1 1.000 0.040 12 26541007 intron variant A/T snv 0.57 0.010 1.000 1 2015 2015
dbSNP: rs4414322
rs4414322
1 1.000 0.040 12 26539038 intron variant C/T snv 0.57 0.010 1.000 1 2015 2015
dbSNP: rs9669395
rs9669395
1 1.000 0.040 12 26538618 intron variant C/T snv 0.57 0.010 1.000 1 2015 2015