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: rs6536024
rs6536024 		1 4 154622217 upstream gene variant T/C snv 0.46 0.800 1.000 1 2013 2013
dbSNP: rs7659024
rs7659024 		2 4 154599778 downstream gene variant G/A snv 0.26 0.800 1.000 1 2011 2011
dbSNP: rs114209171
rs114209171
FUNDC2
5 0.882 0.120 X 155050522 non coding transcript exon variant T/C snv 0.23 0.710 1.000 1 2016 2016
dbSNP: rs1998081
rs1998081
CD93
1 20 23076845 upstream gene variant T/C snv 0.90 0.710 1.000 1 2016 2016
dbSNP: rs10025152
rs10025152
F11-AS1
2 4 186304150 intron variant G/A snv 0.20 0.700 1.000 1 2011 2011
dbSNP: rs10029715
rs10029715
F11-AS1
2 4 186301446 intron variant T/C snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs1008728
rs1008728
F11-AS1
2 4 186305519 intron variant C/T snv 0.57 0.700 1.000 1 2011 2011
dbSNP: rs10090114
rs10090114
MSRA
1 8 10147444 intron variant T/C snv 0.90 0.700 1.000 1 2019 2019
dbSNP: rs1021230
rs1021230
EBF2
1 8 25928927 intron variant A/T snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs10476160
rs10476160 		1 5 175547573 regulatory region variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1048483
rs1048483
HIC1 ; SMG6
1 17 2063163 3 prime UTR variant C/T snv 0.43 0.700 1.000 1 2019 2019
dbSNP: rs10498632
rs10498632
TC2N
2 14 91824400 intron variant A/G snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs10504130
rs10504130
PCMTD1
1 8 51844533 intron variant G/A snv 0.12 0.700 1.000 1 2013 2013
dbSNP: rs10516089
rs10516089
LOC105377724
1 5 171724227 downstream gene variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs10746487
rs10746487 		1 1 9278630 intergenic variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs10747514
rs10747514
PROCR ; MMP24-AS1-EDEM2
1 20 35187566 intron variant G/A snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs10919507
rs10919507 		1 1 170885468 intron variant C/T snv 3.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs11057270
rs11057270
SBNO1
1 12 123323526 intron variant T/C snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs11132387
rs11132387
F11-AS1
1 4 186297569 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs11158204
rs11158204
LOC105370522
1 14 58377808 intron variant C/T snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs113092656
rs113092656 		5 0.882 0.120 6 11615072 intergenic variant G/A snv 2.6E-02 0.700 1.000 1 2016 2016
dbSNP: rs113451833
rs113451833 		1 8 64970119 downstream gene variant G/T snv 0.18 0.700 1.000 1 2019 2019
dbSNP: rs113976843
rs113976843
LINC01681
1 1 170254627 intron variant T/C snv 8.6E-03 0.700 1.000 1 2019 2019
dbSNP: rs114149445
rs114149445
F2RL2 ; IQGAP2
1 5 76625137 intron variant C/T snv 4.7E-03 0.700 1.000 1 2017 2017
dbSNP: rs115063924
rs115063924 		1 1 168741790 intron variant C/A;T snv 6.7E-03 0.700 1.000 1 2019 2019