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: rs17376456
rs17376456
KIAA0825 ; LOC105379087
1 1.000 0.120 5 94221997 intron variant A/G snv 8.7E-02 0.810 1.000 1 2011 2011
dbSNP: rs1571942
rs1571942
PLXDC2
2 0.925 0.160 10 20253705 intron variant A/G snv 0.15 0.800 1.000 1 2011 2011
dbSNP: rs17404956
rs17404956 		1 1.000 0.120 5 166962488 regulatory region variant A/G snv 5.5E-02 0.800 1.000 1 2011 2011
dbSNP: rs2038823
rs2038823
HS6ST3
1 1.000 0.120 13 96299179 intron variant G/A;T snv 0.800 1.000 1 2011 2011
dbSNP: rs2811893
rs2811893
MYSM1
1 1.000 0.120 1 58696476 intron variant T/C snv 0.39 0.800 1.000 1 2011 2011
dbSNP: rs4470583
rs4470583 		1 1.000 0.120 4 161329780 intergenic variant A/G;T snv 0.800 1.000 1 2011 2011
dbSNP: rs476141
rs476141
LINC02774
1 1.000 0.120 1 244013122 intron variant G/A;T snv 0.800 1.000 1 2011 2011
dbSNP: rs4787008
rs4787008
RBFOX1
1 1.000 0.120 16 7365551 intron variant A/G snv 0.87 0.800 1.000 1 2011 2011
dbSNP: rs9866141
rs9866141
LOC101928236
1 1.000 0.120 3 157232790 intron variant C/A;T snv 4.7E-02 0.800 1.000 1 2011 2011
dbSNP: rs11018670
rs11018670 		2 0.925 0.160 11 89623460 intergenic variant A/G snv 0.30 0.700 1.000 1 2018 2018
dbSNP: rs114790220
rs114790220 		1 1.000 0.120 8 5306434 intergenic variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs11662496
rs11662496 		1 1.000 0.120 18 43695432 intergenic variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11771617
rs11771617 		1 1.000 0.120 7 125733372 intergenic variant A/G snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs12656571
rs12656571
MAN2A1
1 1.000 0.120 5 109742339 intron variant G/A snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs142610219
rs142610219
LOC107986902
1 1.000 0.120 8 115906039 intergenic variant A/T snv 2.7E-03 0.700 1.000 1 2019 2019
dbSNP: rs148995025
rs148995025
LINC02196
1 1.000 0.120 5 7085094 intron variant A/G snv 8.9E-03 0.700 1.000 1 2019 2019
dbSNP: rs1535724
rs1535724
LMO7-AS1
1 1.000 0.120 13 75609137 intron variant G/C;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1711347
rs1711347
LINC02774
1 1.000 0.120 1 243998680 intron variant G/A snv 0.53 0.700 1.000 1 2011 2011
dbSNP: rs184340784
rs184340784 		2 0.925 0.160 1 4529823 intergenic variant C/T snv 6.1E-04 0.700 1.000 1 2019 2019
dbSNP: rs200295620
rs200295620 		2 0.925 0.160 3 168172398 intergenic variant T/-;TT delins 5.7E-03 0.700 1.000 1 2019 2019
dbSNP: rs202069793
rs202069793
LOC107987105
1 1.000 0.120 9 104713014 intergenic variant GA/- delins 0.63 0.700 1.000 1 2019 2019
dbSNP: rs2031236
rs2031236
UCHL3
1 1.000 0.120 13 75595641 intron variant G/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs2104455
rs2104455 		1 1.000 0.120 6 9368285 intergenic variant A/G snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs227453
rs227453 		1 1.000 0.120 6 165065309 intron variant A/T snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs227455
rs227455 		1 1.000 0.120 6 165064562 intron variant T/C snv 0.17 0.700 1.000 1 2011 2011