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: rs931608
rs931608
2 1.000 0.040 19 22431320 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10455872
rs10455872
LPA
33 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs1481012
rs1481012
6 0.882 0.200 4 88117930 intron variant A/G snv 8.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs6924995
rs6924995
1 6 16161194 non coding transcript exon variant A/G snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs7412
rs7412
47 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs1875620
rs1875620
1 9 88925144 regulatory region variant G/A snv 0.44 0.700 1.000 1 2012 2012
dbSNP: rs11591147
rs11591147
28 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs7769153
rs7769153
1 6 130935224 intron variant T/G snv 7.2E-02 0.700 1.000 1 2012 2012