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: rs61838774
rs61838774
LYPLAL1 ; LYPLAL1-AS1
1 1 219440433 intron variant A/G snv 0.27 0.700 1.000 1 2017 2017
dbSNP: rs6684375
rs6684375 		4 1 22379941 regulatory region variant C/T snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs6726821
rs6726821 		2 2 165721604 intergenic variant T/G snv 0.40 0.700 1.000 1 2017 2017
dbSNP: rs73169094
rs73169094
DPP6
1 7 154888650 intron variant C/G snv 1.9E-02 0.700 1.000 1 2017 2017
dbSNP: rs7501812
rs7501812
TOM1L2
2 17 17847593 3 prime UTR variant G/A snv 0.47 0.52 0.700 1.000 1 2017 2017
dbSNP: rs754388
rs754388
RIN3
7 0.882 0.120 14 92649065 intron variant G/C;T snv 0.700 1.000 1 2017 2017
dbSNP: rs7672749
rs7672749 		2 4 87877132 intergenic variant G/A snv 0.11 0.700 1.000 1 2017 2017
dbSNP: rs775327225
rs775327225 		1 X 100764930 intergenic variant T/C snv 5.3E-04 0.700 1.000 1 2017 2017
dbSNP: rs917727
rs917727
FAM3C
3 7 121378525 intron variant C/A;T snv 0.33 0.700 1.000 1 2017 2017
dbSNP: rs9525638
rs9525638 		3 13 42554441 regulatory region variant T/C snv 0.37 0.700 1.000 1 2017 2017
dbSNP: rs9936385
rs9936385
FTO
5 0.925 0.120 16 53785257 intron variant T/C snv 0.41 0.700 1.000 1 2017 2017
dbSNP: rs9972653
rs9972653
FTO
2 16 53780451 intron variant G/T snv 0.40 0.700 1.000 1 2017 2017
dbSNP: rs9991501
rs9991501
HSD17B11
1 4 87337331 missense variant C/T snv 2.3E-02 0.700 1.000 1 2017 2017
dbSNP: rs10068807
rs10068807 		1 5 55581157 intergenic variant A/G snv 0.70 0.700 1.000 1 2019 2019
dbSNP: rs10269139
rs10269139
GLI3
1 7 42108589 intron variant C/T snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs10433500
rs10433500
CADM2
1 3 85497648 intron variant G/A snv 0.51 0.700 1.000 1 2019 2019
dbSNP: rs1047891
rs1047891
CPS1
34 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 0.700 1.000 1 2019 2019
dbSNP: rs10917220
rs10917220 		1 1 22356912 intergenic variant T/C snv 0.65 0.700 1.000 1 2019 2019
dbSNP: rs10938397
rs10938397 		19 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs11001398
rs11001398
LRMDA
1 10 75461756 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs11014285
rs11014285
PRTFDC1
2 10 24889935 intron variant G/A snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs11030119
rs11030119
BDNF
3 11 27706555 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1108548
rs1108548
LINC02869
1 1 218461445 intron variant A/G snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs11128264
rs11128264 		1 3 72343159 intergenic variant C/T snv 0.55 0.700 1.000 1 2019 2019
dbSNP: rs111352324
rs111352324
FAF1
1 1 50755008 intron variant T/C snv 8.7E-02 0.700 1.000 1 2019 2019