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: rs10512148
rs10512148
1 9 84494571 intron variant A/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs1077625
rs1077625
1 9 84519729 intron variant A/G snv 3.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs113847670
rs113847670
2 10 127076415 intron variant C/T snv 3.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs13295359
rs13295359
1 9 84558757 intron variant C/T snv 3.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs13295556
rs13295556
1 9 84493940 intron variant C/T snv 4.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs13297129
rs13297129
1 9 84494136 intron variant T/C snv 4.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs1409705
rs1409705
1 9 84491947 intron variant G/C snv 4.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs17046216
rs17046216
1 4 165334552 intron variant T/A snv 0.35 0.800 1.000 1 2012 2012
dbSNP: rs17346028
rs17346028
1 9 84557432 intron variant G/A snv 3.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs17346170
rs17346170
1 9 84560886 intron variant A/G snv 3.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs17346477
rs17346477
1 9 84568293 intron variant C/A;G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs17430135
rs17430135
1 9 84497421 intron variant A/G snv 4.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs17430887
rs17430887
1 9 84560801 intron variant T/C snv 3.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs17431357
rs17431357
1 12 120442631 intron variant C/T snv 4.5E-02 0.800 1.000 1 2011 2011
dbSNP: rs17488534
rs17488534
1 4 165334788 intron variant G/A snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs2118496
rs2118496
1 4 165333821 intron variant A/G snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs34273676
rs34273676
1 9 84496052 intron variant T/A snv 4.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs34289003
rs34289003
1 9 84557293 intron variant A/T snv 3.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs34307009
rs34307009
1 9 84512008 intron variant A/G snv 4.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs34439305
rs34439305
1 9 84511589 intron variant A/G snv 4.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs34629677
rs34629677
1 9 84512042 intron variant C/T snv 4.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs34808171
rs34808171
1 9 84503715 intron variant C/G snv 4.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs35060039
rs35060039
1 9 84493809 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs35640669
rs35640669
1 9 84562671 intron variant T/C snv 3.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs35842364
rs35842364
1 9 84518341 intron variant G/A snv 4.2E-02 0.700 1.000 1 2012 2012