Source: ALL
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: rs34439305
rs34439305
LOC102724036
1 9 84511589 intron variant A/G snv 4.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs34629677
rs34629677
LOC102724036
1 9 84512042 intron variant C/T snv 4.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs34808171
rs34808171
LOC102724036
1 9 84503715 intron variant C/G snv 4.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs35060039
rs35060039
LOC102724036
1 9 84493809 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs35640669
rs35640669
LOC102724036
1 9 84562671 intron variant T/C snv 3.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs35842364
rs35842364
LOC102724036
1 9 84518341 intron variant G/A snv 4.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs3904480
rs3904480
LOC102724036
1 9 84498383 intron variant T/A snv 4.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs3904481
rs3904481
LOC102724036
1 9 84498579 intron variant G/A snv 4.1E-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: rs4463503
rs4463503
LOC102724036
1 9 84498612 intron variant A/G snv 4.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs62519907
rs62519907 		2 8 71696834 intron variant G/A;T snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs7020767
rs7020767
LOC102724036
1 9 84504913 intron variant C/T snv 4.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs7029848
rs7029848
LOC102724036
1 9 84499953 intron variant A/G snv 4.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs7077836
rs7077836 		1 10 130953235 intergenic variant G/A snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs7468189
rs7468189
LOC102724036
1 9 84504186 intron variant T/C 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: rs7856875
rs7856875
LOC102724036
1 9 84512625 intron variant C/T snv 4.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs7864887
rs7864887
LOC102724036
1 9 84507168 intron variant C/T snv 4.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs8093427
rs8093427 		1 18 39191160 intergenic variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs9396607
rs9396607 		1 6 15855197 intergenic variant G/T snv 2.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs9524298
rs9524298
GPC6
1 13 93980567 intron variant G/A snv 0.17 0.700 1.000 1 2012 2012
dbSNP: rs1014959895
rs1014959895
PRMT7
16 0.763 0.360 16 68329105 stop gained G/C;T snv 4.0E-06; 1.6E-05 0.700 0
dbSNP: rs121913139
rs121913139
INSR
2 1.000 0.120 19 7122662 missense variant C/T snv 0.700 0
dbSNP: rs121913157
rs121913157
INSR
1 19 7120739 missense variant C/T snv 0.700 0
dbSNP: rs1251713297
rs1251713297
PRMT7
15 0.776 0.360 16 68355785 stop gained C/A snv 8.1E-06 0.700 0