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 1 2011 2011
dbSNP: rs633185
rs633185
ARHGAP42
10 0.925 0.080 11 100722807 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs7129220
rs7129220
AMPD3 ; CAND1.11
5 11 10328991 intron variant G/A snv 0.10 0.700 1.000 1 2011 2011
dbSNP: rs805303
rs805303
BAG6
7 0.925 0.160 6 31648589 intron variant G/A snv 0.45 0.700 1.000 1 2011 2011
dbSNP: rs932764
rs932764
PLCE1
6 10 94136183 intron variant A/G snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs10504249
rs10504249
LINC01602 ; LOC105375856
3 8 57876522 intron variant A/G snv 1.7E-02 0.700 1.000 1 2013 2013
dbSNP: rs10930597
rs10930597 		3 2 173462117 intergenic variant C/T snv 0.14 0.700 1.000 1 2013 2013
dbSNP: rs11867410
rs11867410
APOH
3 17 66231245 intron variant T/C snv 4.0E-02 0.700 1.000 1 2013 2013
dbSNP: rs11887188
rs11887188 		3 2 234394166 intergenic variant C/T snv 0.11 0.700 1.000 1 2013 2013
dbSNP: rs13067306
rs13067306 		2 3 94524869 regulatory region variant G/A snv 0.17 0.700 1.000 1 2013 2013
dbSNP: rs1330225
rs1330225 		3 1 106293321 intergenic variant T/C snv 0.38 0.700 1.000 1 2013 2013
dbSNP: rs17135875
rs17135875
FBXL13
3 7 102878584 intron variant T/C snv 0.24 0.700 1.000 1 2013 2013
dbSNP: rs2030114
rs2030114
HNRNPA1P48
2 16 51576036 intron variant G/A snv 0.23 0.700 1.000 1 2013 2013
dbSNP: rs2627282
rs2627282
LOC105377786
3 8 2923434 upstream gene variant G/A snv 0.25 0.700 1.000 1 2013 2013
dbSNP: rs7286472
rs7286472 		2 22 33990484 intergenic variant A/G snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs4601790
rs4601790
EHBP1L1
4 11 65586435 intron variant A/G snv 0.23 0.700 1.000 1 2014 2014
dbSNP: rs10275663
rs10275663
GRB10
2 7 50729988 intron variant G/A snv 9.4E-02 0.700 1.000 1 2015 2015
dbSNP: rs148514273
rs148514273
SETD7
2 4 139543924 intron variant G/A snv 2.4E-02 0.700 1.000 1 2017 2017
dbSNP: rs10059884
rs10059884 		5 5 32832368 regulatory region variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10255839
rs10255839
EVX1
6 7 27249498 intron variant G/A snv 0.87 0.700 1.000 1 2018 2018
dbSNP: rs10743353
rs10743353
LINC02398
2 12 20047028 intron variant C/T snv 0.60 0.700 1.000 1 2018 2018
dbSNP: rs11065979
rs11065979 		12 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 0.700 1.000 1 2018 2018
dbSNP: rs11099097
rs11099097 		6 4 80246155 intergenic variant C/T snv 0.30 0.700 1.000 1 2018 2018
dbSNP: rs11725969
rs11725969
GUCY1A1
5 4 155705436 intron variant C/T snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs1275986
rs1275986 		2 2 26689211 upstream gene variant C/A snv 0.50 0.700 1.000 1 2018 2018