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: rs10512148
rs10512148
LOC102724036
1 9 84494571 intron variant A/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs17346477
rs17346477
LOC102724036
1 9 84568293 intron variant C/A;G;T snv 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: rs8093427
rs8093427 		1 18 39191160 intergenic variant T/A;C snv 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
dbSNP: rs1568426700
rs1568426700
INSR
1 19 7120678 missense variant G/A snv 0.700 0
dbSNP: rs886041065
rs886041065
ASXL2
43 0.677 0.600 2 25743913 frameshift variant G/- delins 0.700 0
dbSNP: rs199560195
rs199560195
TBC1D4
1 13 75299364 missense variant C/A;T snv 3.6E-05 2.8E-05 0.700 0
dbSNP: rs77164426
rs77164426 		2 2 146756888 intergenic variant A/G snv 1.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs9396607
rs9396607 		1 6 15855197 intergenic variant G/T snv 2.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs17254590
rs17254590 		2 13 106384996 downstream gene variant G/C snv 2.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs113847670
rs113847670
DOCK1
2 10 127076415 intron variant C/T snv 3.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs35640669
rs35640669
LOC102724036
1 9 84562671 intron variant T/C snv 3.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs13295359
rs13295359
LOC102724036
1 9 84558757 intron variant C/T snv 3.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs17346170
rs17346170
LOC102724036
1 9 84560886 intron variant A/G snv 3.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs34289003
rs34289003
LOC102724036
1 9 84557293 intron variant A/T snv 3.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs17430887
rs17430887
LOC102724036
1 9 84560801 intron variant T/C snv 3.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs17346028
rs17346028
LOC102724036
1 9 84557432 intron variant G/A snv 3.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs1077625
rs1077625
LOC102724036
1 9 84519729 intron variant A/G snv 3.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs7020767
rs7020767
LOC102724036
1 9 84504913 intron variant C/T snv 4.1E-02 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: rs34273676
rs34273676
LOC102724036
1 9 84496052 intron variant T/A snv 4.1E-02 0.700 1.000 1 2012 2012