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: rs10858740
rs10858740 		5 12 88451258 intergenic variant A/G;T snv 0.56 0.700 1.000 1 2016 2016
dbSNP: rs10864462
rs10864462
PEX14
1 1 10552101 intron variant A/T snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs10882899
rs10882899
FRAT2 ; LOC105378448
1 10 97336188 intron variant G/C snv 0.49 0.700 1.000 1 2019 2019
dbSNP: rs10899789
rs10899789
LINC02633 ; LOC105378271
1 10 43322411 upstream gene variant C/G snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs10905284
rs10905284
GATA3
4 0.882 0.200 10 8073399 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10934582
rs10934582 		3 3 122294507 downstream gene variant G/A snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs10956401
rs10956401
PVT1
1 8 127990173 non coding transcript exon variant G/A snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs10956483
rs10956483
CCDC26
3 8 129559864 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs10980457
rs10980457
SVEP1
1 9 110576455 intron variant A/C snv 9.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs10982456
rs10982456
TNFSF8 ; DELEC1
1 9 114928478 intron variant T/C snv 0.57 0.700 1.000 1 2019 2019
dbSNP: rs1099448
rs1099448
TNFSF4 ; LOC100506023
1 1 173262759 intergenic variant C/T snv 0.58 0.700 1.000 1 2019 2019
dbSNP: rs10995240
rs10995240
ZNF365 ; LOC105378327
2 10 62628871 intron variant G/C snv 0.29 0.700 1.000 1 2016 2016
dbSNP: rs10995477
rs10995477
JMJD1C
4 10 63250912 intron variant T/C snv 0.43 0.700 1.000 1 2016 2016
dbSNP: rs11010134
rs11010134
LINC02634
1 10 35229101 intron variant A/G snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs11014291
rs11014291
PRTFDC1
1 10 24909758 intron variant T/C snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs11018874
rs11018874
NAALAD2
2 11 90142269 intron variant G/A snv 9.7E-02 0.700 1.000 1 2011 2011
dbSNP: rs11055989
rs11055989
ATF7IP
1 12 14469068 intron variant A/G snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs1105935
rs1105935
KIAA2012
1 2 202161307 intron variant T/A;C snv 0.14 0.700 1.000 1 2019 2019
dbSNP: rs11068852
rs11068852
TCHP
1 12 109904616 intron variant T/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs11071559
rs11071559
RORA
4 0.925 0.080 15 60777789 intron variant C/T snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs11077961
rs11077961 		1 17 83054873 upstream gene variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11082513
rs11082513 		3 18 46167187 intergenic variant C/T snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs11084096
rs11084096
SIGLEC5
1 19 51625542 intron variant G/A snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs1109151
rs1109151
ZC3H7B
1 22 41356940 intron variant A/G snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs11106430
rs11106430
LINC01619
1 12 92118652 intron variant C/A;T snv 0.700 1.000 1 2019 2019