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: rs1533326
rs1533326
SEMA4B
1 1.000 0.040 15 90211722 intron variant A/G snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs28570522
rs28570522
PINX1 ; LOC102723313
1 1.000 0.040 8 10773058 intron variant A/G snv 0.66 0.700 1.000 1 2018 2018
dbSNP: rs2901000
rs2901000 		1 1.000 0.040 2 60274081 intergenic variant A/G snv 0.62 0.700 1.000 1 2018 2018
dbSNP: rs38055
rs38055 		1 1.000 0.040 5 53264814 intergenic variant A/G snv 0.75 0.700 1.000 1 2014 2014
dbSNP: rs6428829
rs6428829
HSD3B1
2 0.925 0.040 1 119512118 intron variant A/G snv 0.78 0.010 1.000 1 2013 2013
dbSNP: rs10911268
rs10911268 		1 1.000 0.040 1 183153583 intergenic variant C/A snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs788790
rs788790 		1 1.000 0.040 1 202320478 downstream gene variant C/A snv 0.44 0.700 1.000 1 2018 2018
dbSNP: rs1801282
rs1801282
PPARG
131 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.020 1.000 2 2014 2018
dbSNP: rs1805192
rs1805192
PPARG
121 0.510 0.840 3 12379739 missense variant C/G snv 0.020 1.000 2 2014 2018
dbSNP: rs11118336
rs11118336
LYPLAL1-AS1
1 1.000 0.040 1 219547941 intergenic variant C/T snv 0.51 0.700 1.000 1 2018 2018
dbSNP: rs2242095
rs2242095
EEF1D ; TIGD5
1 1.000 0.040 8 143596704 5 prime UTR variant C/T snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs34560261
rs34560261
SEMA4B
3 0.882 0.040 15 90191194 intron variant C/T snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs72966077
rs72966077
WNT10A ; LOC105373882
1 1.000 0.040 2 218894507 intron variant C/T snv 3.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs747650
rs747650
C11orf49
1 1.000 0.040 11 47154454 non coding transcript exon variant C/T snv 0.34 0.700 1.000 1 2014 2014
dbSNP: rs1159268
rs1159268 		1 1.000 0.040 1 218671564 regulatory region variant G/A snv 0.32 0.700 1.000 1 2014 2014
dbSNP: rs158639
rs158639
LOC105378977
1 1.000 0.040 5 56315883 intron variant G/A snv 0.33 0.700 1.000 1 2018 2018
dbSNP: rs330071
rs330071 		1 1.000 0.040 8 9302385 intron variant G/A snv 0.25 0.700 1.000 1 2014 2014
dbSNP: rs4487353
rs4487353 		1 1.000 0.040 4 123332634 intergenic variant G/A snv 0.53 0.700 1.000 1 2018 2018
dbSNP: rs5743708
rs5743708
TLR2
98 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 0.010 1.000 1 2010 2010
dbSNP: rs6684868
rs6684868 		1 1.000 0.040 1 218674648 TF binding site variant G/A snv 0.41 0.700 1.000 1 2018 2018
dbSNP: rs7531806
rs7531806
C1orf112 ; LOC107985745
1 1.000 0.040 1 169681903 intron variant G/A snv 0.61 0.700 1.000 1 2014 2014
dbSNP: rs75430906
rs75430906 		1 1.000 0.040 3 20676437 intron variant G/A snv 1.9E-02 0.700 1.000 1 2014 2014
dbSNP: rs7799039
rs7799039
LOC105375494
33 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 0.010 1.000 1 2018 2018
dbSNP: rs2727365
rs2727365 		1 1.000 0.040 11 13089937 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1092479
rs1092479 		1 1.000 0.040 2 121011861 intergenic variant G/C snv 0.39 0.700 1.000 1 2018 2018