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: rs1024611
rs1024611 		63 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.010 1.000 1 2019 2019
dbSNP: rs103294
rs103294 		7 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 0.010 1.000 1 2013 2013
dbSNP: rs10786938
rs10786938 		1 1.000 0.040 10 106280012 intergenic variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10983755
rs10983755 		7 0.790 0.320 9 117702392 upstream gene variant G/A snv 3.2E-02 0.010 1.000 1 2019 2019
dbSNP: rs11084596
rs11084596 		3 1.000 0.040 19 31614073 regulatory region variant T/C snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs11199879
rs11199879 		3 1.000 0.040 10 121285698 regulatory region variant T/C snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs12826786
rs12826786 		26 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.010 1.000 1 2017 2017
dbSNP: rs141179786
rs141179786 		1 1.000 0.040 18 53662174 intergenic variant A/G;T snv 2.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs148678804
rs148678804 		2 1.000 0.040 10 22138360 intergenic variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs16902947
rs16902947 		1 1.000 0.040 5 36308995 intergenic variant A/G snv 0.22 0.010 1.000 1 2017 2017
dbSNP: rs17144046
rs17144046 		4 0.882 0.120 10 8564051 intergenic variant A/G snv 0.28 0.700 1.000 1 2017 2017
dbSNP: rs200476
rs200476 		2 1.000 0.040 6 27800570 intergenic variant A/T snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs2555019
rs2555019 		3 1.000 0.040 12 114230813 intergenic variant T/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs2735839
rs2735839 		7 0.827 0.160 19 50861367 upstream gene variant A/C;G snv 0.010 1.000 1 2019 2019
dbSNP: rs6078585
rs6078585 		1 1.000 0.040 20 12447612 intergenic variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs7906649
rs7906649 		2 1.000 0.040 10 22021369 intergenic variant G/A snv 0.60 0.700 1.000 1 2018 2018
dbSNP: rs1034866440
rs1034866440
AR
4 0.851 0.160 X 67643401 missense variant G/A snv 5.7E-06 0.010 1.000 1 2005 2005
dbSNP: rs137852569
rs137852569
AR
10 0.752 0.320 X 67686030 missense variant G/A snv 9.4E-06 0.010 1.000 1 2005 2005
dbSNP: rs6152
rs6152
AR
9 0.763 0.240 X 67545785 synonymous variant G/A snv 0.15 0.28 0.010 1.000 1 2015 2015
dbSNP: rs3803185
rs3803185
ARL11
19 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 0.010 1.000 1 2011 2011
dbSNP: rs2556378
rs2556378
BCL11A
3 1.000 0.040 2 60535367 3 prime UTR variant T/G snv 0.81 0.700 1.000 1 2018 2018
dbSNP: rs72878024
rs72878024
BET1L ; ODF3
2 1.000 0.040 11 199492 missense variant G/A snv 6.4E-02 6.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs4938723
rs4938723
BTG4 ; MIR34B ; MIR34C ; LOC728196
60 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2017 2017
dbSNP: rs10035432
rs10035432
C5orf46
1 1.000 0.040 5 147855193 upstream gene variant G/A snv 0.18 0.010 1.000 1 2015 2015
dbSNP: rs677394
rs677394
C5orf66
2 1.000 0.040 5 135271869 intron variant G/C;T snv 0.700 1.000 1 2018 2018