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: rs700755
rs700755
TNS3
3 0.882 0.040 7 47406044 intron variant A/G snv 0.47 0.700 1.000 1 2019 2019
dbSNP: rs2151280
rs2151280
CDKN2B-AS1
16 0.701 0.360 9 22034720 non coding transcript exon variant G/A snv 0.46 0.700 1.000 2 2014 2015
dbSNP: rs10896064
rs10896064
EFEMP2
3 0.882 0.040 11 65873562 5 prime UTR variant G/C snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs35540156
rs35540156
FOXP1
3 0.882 0.040 3 71473027 intron variant A/G snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs109077
rs109077
PPARGC1B
3 0.882 0.040 5 149817119 intron variant T/G snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs4710154
rs4710154 		3 0.882 0.040 6 166981146 intron variant A/T snv 0.42 0.700 1.000 2 2016 2019
dbSNP: rs7776701
rs7776701
TNS3
3 0.882 0.040 7 47403036 intron variant T/C snv 0.40 0.700 1.000 1 2016 2016
dbSNP: rs11993814
rs11993814 		3 0.882 0.040 8 80477556 intron variant C/T snv 0.39 0.700 1.000 1 2016 2016
dbSNP: rs2776353
rs2776353
LOC105372813 ; LOC107985478
3 0.882 0.040 21 41668857 regulatory region variant A/T snv 0.39 0.700 1.000 2 2016 2019
dbSNP: rs7538876
rs7538876
PADI6
6 0.807 0.120 1 17395867 intron variant G/A snv 0.37 0.700 1.000 3 2008 2015
dbSNP: rs231726
rs231726 		7 0.790 0.200 2 203876143 downstream gene variant C/T snv 0.36 0.700 1.000 1 2019 2019
dbSNP: rs7528427
rs7528427
RCC2
3 0.882 0.040 1 17419777 intron variant C/T snv 0.36 0.700 1.000 1 2019 2019
dbSNP: rs11719821
rs11719821
LPP
3 0.882 0.040 3 188370530 intron variant T/C snv 0.36 0.700 1.000 1 2019 2019
dbSNP: rs59586681
rs59586681 		4 0.851 0.040 20 2239664 intron variant A/G;T snv 0.34 0.700 1.000 1 2014 2014
dbSNP: rs1246946
rs1246946 		4 0.851 0.040 6 4979722 downstream gene variant C/T snv 0.34 0.700 1.000 1 2019 2019
dbSNP: rs7508601
rs7508601
SCAF1
3 0.882 0.040 19 49648429 intron variant T/A snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs7620634
rs7620634
ST3GAL6-AS1
3 0.882 0.040 3 98728296 intron variant G/A snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs61824911
rs61824911 		3 0.882 0.040 1 228843990 intergenic variant A/G snv 0.30 0.700 1.000 1 2016 2016
dbSNP: rs16917546
rs16917546
ZNF365 ; LOC105378327
6 0.851 0.040 10 62637778 intron variant T/C snv 0.29 0.700 1.000 1 2017 2017
dbSNP: rs10995255
rs10995255
ZNF365 ; LOC105378327
3 0.882 0.040 10 62642673 intron variant G/A snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs157935
rs157935
LINC-PINT ; LINC00513
4 0.851 0.040 7 130900794 intron variant T/G snv 0.28 0.700 1.000 2 2014 2015
dbSNP: rs10102591
rs10102591 		3 0.882 0.040 8 80479448 intron variant G/T snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs125124
rs125124
LINC-PINT ; LINC00513
3 0.882 0.040 7 130899925 intron variant C/G snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs7907606
rs7907606 		8 0.790 0.120 10 103920874 upstream gene variant T/G snv 0.26 0.700 1.000 1 2016 2016
dbSNP: rs663743
rs663743
CCDC88B ; LOC102723878
5 0.827 0.120 11 64340263 5 prime UTR variant G/A snv 0.33 0.25 0.700 1.000 1 2019 2019