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: rs11724635
rs11724635
3 0.925 0.080 4 15735478 intron variant C/A;G snv 0.43 0.880 0.846 13 2011 2019
dbSNP: rs4698412
rs4698412
1 1.000 0.040 4 15735725 intron variant G/A;T snv 0.850 1.000 7 2011 2019
dbSNP: rs4538475
rs4538475
2 1.000 0.040 4 15736314 intron variant A/G snv 0.24 0.810 1.000 3 2009 2012
dbSNP: rs11931532
rs11931532
1 1.000 0.040 4 15724143 intron variant T/C snv 0.13 0.730 0.500 4 2012 2019
dbSNP: rs12645693
rs12645693
1 1.000 0.040 4 15727911 intron variant G/A snv 8.1E-02 0.710 0.500 2 2012 2012
dbSNP: rs3213710
rs3213710
1 1.000 0.040 4 15715698 intron variant G/A snv 0.52 0.44 0.700 1.000 1 2012 2012
dbSNP: rs4266290
rs4266290
1 1.000 0.040 4 15735495 intron variant G/C snv 0.33 0.700 1.000 1 2016 2016
dbSNP: rs12502586
rs12502586
1 1.000 0.040 4 15724941 intron variant G/A snv 7.0E-02 0.020 1.000 2 2011 2011