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: rs6015450
rs6015450
ZNF831
7 20 59176062 intron variant A/G snv 0.14 0.700 1.000 4 2011 2018
dbSNP: rs11065979
rs11065979 		12 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 0.700 1.000 3 2016 2019
dbSNP: rs11066280
rs11066280
HECTD4
27 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.700 1.000 3 2011 2015
dbSNP: rs11191548
rs11191548
CNNM2
10 0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02 0.700 1.000 3 2011 2018
dbSNP: rs1530440
rs1530440
CABCOCO1
6 1.000 0.040 10 61764833 intron variant C/T snv 0.15 0.700 1.000 3 2009 2018
dbSNP: rs167479
rs167479
RGL3
5 19 11416089 missense variant T/A;C;G snv 0.700 1.000 3 2016 2017
dbSNP: rs16948048
rs16948048
ZNF652 ; LOC102724596
8 0.925 0.040 17 49363104 intron variant A/G snv 0.37 0.700 1.000 3 2009 2017
dbSNP: rs17030613
rs17030613
CAPZA1
7 1 112648185 intron variant A/C snv 0.19 0.700 1.000 3 2011 2018
dbSNP: rs1801253
rs1801253
ADRB1
34 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.700 1.000 3 2017 2018
dbSNP: rs1887320
rs1887320 		6 20 10985350 intron variant G/A snv 0.46 0.700 1.000 3 2015 2018
dbSNP: rs1902859
rs1902859 		4 4 80236549 regulatory region variant T/C snv 0.27 0.700 1.000 3 2015 2019
dbSNP: rs2586886
rs2586886
KCNK3
4 1.000 0.080 2 26709163 intron variant C/G;T snv 0.700 1.000 3 2016 2019
dbSNP: rs2932538
rs2932538
MOV10
4 1 112673921 intron variant A/C;G snv 0.700 1.000 3 2011 2017
dbSNP: rs35443
rs35443 		5 12 115115073 intergenic variant G/C snv 0.40 0.700 1.000 3 2018 2018
dbSNP: rs4247374
rs4247374
INSR
2 19 7252745 intron variant C/T snv 9.7E-02 0.700 1.000 3 2016 2018
dbSNP: rs6495122
rs6495122 		6 1.000 0.040 15 74833304 downstream gene variant A/C snv 0.44 0.700 1.000 3 2009 2018
dbSNP: rs653178
rs653178
ATXN2
41 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 3 2009 2019
dbSNP: rs7599598
rs7599598
FER1L5
2 2 96686103 missense variant A/G;T snv 0.41 0.700 1.000 3 2017 2018
dbSNP: rs900145
rs900145 		4 11 13272358 upstream gene variant C/T snv 0.62 0.700 1.000 3 2016 2018
dbSNP: rs932764
rs932764
PLCE1
6 10 94136183 intron variant A/G snv 0.38 0.700 1.000 3 2011 2017
dbSNP: rs9815354
rs9815354
ULK4
4 0.925 0.160 3 41871159 intron variant G/A;T snv 0.700 1.000 3 2009 2017
dbSNP: rs10077885
rs10077885 		2 5 115054424 regulatory region variant C/A snv 0.56 0.700 1.000 2 2016 2018
dbSNP: rs10184428
rs10184428 		5 2 164155317 intron variant C/A;G snv 0.700 1.000 2 2018 2018
dbSNP: rs1063281
rs1063281
TNS1
2 2 217804009 3 prime UTR variant C/A;T snv 0.700 1.000 2 2017 2017
dbSNP: rs10776752
rs10776752
WNT2B
4 1 112501706 intron variant G/T snv 8.8E-02 0.700 1.000 2 2018 2018