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: rs4810485
rs4810485
CD40
16 0.732 0.480 20 46119308 intron variant T/A;G snv 0.710 1.000 2 2011 2016
dbSNP: rs6679677
rs6679677
PHTF1
26 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.710 1.000 2 2012 2015
dbSNP: rs917997
rs917997 		20 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 0.710 1.000 2 2011 2013
dbSNP: rs10202630
rs10202630 		4 0.882 2 190398199 intergenic variant T/C snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs1032129
rs1032129
TNFRSF11B
5 0.851 0.040 8 118939661 intron variant A/C snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs10425559
rs10425559 		7 0.807 0.040 19 4837475 upstream gene variant A/G snv 0.66 0.700 1.000 1 2019 2019
dbSNP: rs10444776
rs10444776
LOC112268138
4 0.882 14 105647030 upstream gene variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10460003
rs10460003
LINC01882
2 18 12747013 intron variant C/T snv 0.15 0.700 1.000 1 2011 2011
dbSNP: rs10488631
rs10488631
TNPO3
13 0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 0.700 1.000 1 2011 2011
dbSNP: rs10494079
rs10494079
VAV3
4 0.882 1 107832253 intron variant G/C snv 9.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs10748781
rs10748781 		11 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs10752747
rs10752747
MMEL1
2 1 2593476 intron variant G/T snv 0.41 0.700 1.000 1 2011 2011
dbSNP: rs10797431
rs10797431
LOC100996583
5 0.851 0.080 1 2569783 non coding transcript exon variant G/T snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs10806425
rs10806425
BACH2
6 0.851 0.280 6 90216893 intron variant C/A snv 0.33 0.700 1.000 1 2011 2011
dbSNP: rs10822050
rs10822050 		14 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 0.700 1.000 1 2015 2015
dbSNP: rs10892258
rs10892258
LOC105369519
4 0.925 0.120 11 118709156 intron variant G/A snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs10892286
rs10892286
DDX6
2 11 118771376 intron variant A/C snv 0.17 0.700 1.000 1 2011 2011
dbSNP: rs10903122
rs10903122 		5 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 0.700 1.000 1 2011 2011
dbSNP: rs10932019
rs10932019 		2 2 203764087 downstream gene variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs10937560
rs10937560
MB21D2
4 0.882 3 192909627 intron variant G/C snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs10986284
rs10986284 		4 0.882 9 124236874 intergenic variant A/T snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs10988542
rs10988542
FNBP1
14 0.724 0.240 9 129894985 intron variant G/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs11043097
rs11043097
LINC02752
2 11 11114248 intron variant T/C snv 0.15 0.700 1.000 1 2011 2011
dbSNP: rs11073337
rs11073337
RASGRP1
5 0.851 0.040 15 38555562 intron variant A/C snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs11086102
rs11086102 		6 0.882 19 18287818 upstream gene variant G/C snv 0.64 0.700 1.000 1 2019 2019