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: rs1217691063
rs1217691063
MTHFR
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.020 0.500 2 2012 2013
dbSNP: rs1801275
rs1801275
IL4R
58 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 0.020 < 0.001 2 2013 2014
dbSNP: rs731236
rs731236
VDR
81 0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 0.020 1.000 2 2013 2020
dbSNP: rs10468514
rs10468514 		1 1.000 0.040 17 45378874 intergenic variant A/G snv 0.38 0.700 1.000 1 2019 2019
dbSNP: rs10756796
rs10756796
BNC2
1 1.000 0.040 9 16730976 intron variant A/G snv 0.43 0.700 1.000 1 2019 2019
dbSNP: rs10991797
rs10991797
LINC00484
1 1.000 0.040 9 91168389 intron variant A/G snv 0.71 0.700 1.000 1 2019 2019
dbSNP: rs10993994
rs10993994
MSMB
15 0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54 0.700 1.000 1 2019 2019
dbSNP: rs11204971
rs11204971
FLG-AS1
2 0.925 0.120 1 152286602 intron variant A/G snv 0.15 0.010 1.000 1 2012 2012
dbSNP: rs112111458
rs112111458 		2 0.925 0.120 2 70872975 intergenic variant A/G snv 0.16 0.010 1.000 1 2017 2017
dbSNP: rs12068304
rs12068304
BATF3
1 1.000 0.040 1 212691650 intron variant A/G snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs12152276
rs12152276
PIGX ; NRROS
1 1.000 0.040 3 196641630 intron variant A/G snv 5.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs1295685
rs1295685
IL13 ; TH2LCRR
7 0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 0.700 1.000 1 2019 2019
dbSNP: rs13277355
rs13277355 		3 0.882 0.120 8 127765473 intergenic variant A/G snv 0.71 0.700 1.000 1 2019 2019
dbSNP: rs13323006
rs13323006 		1 1.000 0.040 3 112904703 regulatory region variant A/G snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs13360927
rs13360927
TMEM232
3 0.882 0.160 5 110700055 intron variant A/G snv 9.3E-02 0.010 1.000 1 2012 2012
dbSNP: rs17669032
rs17669032
PTPRC
1 1.000 0.040 1 198684045 intron variant A/G snv 7.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs17718511
rs17718511
SPINK5
2 0.925 0.120 5 148072009 intron variant A/G snv 3.2E-02 0.010 1.000 1 2010 2010
dbSNP: rs2066446
rs2066446
IL12RB2
2 0.925 0.120 1 67315434 intron variant A/G snv 0.20 0.010 1.000 1 2010 2010
dbSNP: rs2158177
rs2158177
TH2LCRR
5 0.925 0.120 5 132648366 intron variant A/G snv 0.18 0.010 1.000 1 2017 2017
dbSNP: rs2455101
rs2455101
PRDM16
1 1.000 0.040 1 3259164 intron variant A/G snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs2569190
rs2569190
CD14 ; TMCO6
39 0.620 0.560 5 140633331 intron variant A/G snv 0.57 0.010 1.000 1 2005 2005
dbSNP: rs28441202
rs28441202
RPTN ; PUDPP2
2 0.925 0.120 1 152156387 missense variant A/G snv 0.010 1.000 1 2017 2017
dbSNP: rs3116590
rs3116590
DLEU1
1 1.000 0.040 13 50234741 intron variant A/G snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs343473
rs343473 		1 1.000 0.040 9 6074936 regulatory region variant A/G snv 0.68 0.700 1.000 1 2019 2019
dbSNP: rs3756094
rs3756094
IRF2
2 0.925 0.120 4 184429780 intron variant A/G snv 0.66 0.010 1.000 1 2012 2012