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: rs17346170
rs17346170
1 9 84560886 intron variant A/G snv 3.4E-02 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: rs2118496
rs2118496
1 4 165333821 intron variant A/G snv 0.57 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: rs4463503
rs4463503
1 9 84498612 intron variant A/G snv 4.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs7029848
rs7029848
1 9 84499953 intron variant A/G snv 4.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs77164426
rs77164426
2 2 146756888 intergenic variant A/G snv 1.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs34289003
rs34289003
1 9 84557293 intron variant A/T snv 3.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs1251713297
rs1251713297
15 0.776 0.360 16 68355785 stop gained C/A snv 8.1E-06 0.700 0
dbSNP: rs17346477
rs17346477
1 9 84568293 intron variant C/A;G;T snv 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: rs199560195
rs199560195
1 13 75299364 missense variant C/A;T snv 3.6E-05 2.8E-05 0.700 0
dbSNP: rs34808171
rs34808171
1 9 84503715 intron variant C/G snv 4.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs10829848
rs10829848
1 10 130949624 intergenic variant C/T snv 0.15 0.800 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: rs17431357
rs17431357
1 12 120442631 intron variant C/T snv 4.5E-02 0.800 1.000 1 2011 2011
dbSNP: rs34629677
rs34629677
1 9 84512042 intron variant C/T snv 4.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs4427876
rs4427876
1 18 39171334 intergenic variant C/T snv 0.75 0.700 1.000 1 2012 2012
dbSNP: rs7020767
rs7020767
1 9 84504913 intron variant C/T snv 4.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs7856875
rs7856875
1 9 84512625 intron variant C/T snv 4.2E-02 0.700 1.000 1 2012 2012