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: rs13191519
rs13191519
HLA-B ; LINC02571 ; LOC112267902
4 1.000 6 31297975 intron variant T/C snv 0.12 0.700 1.000 1 2009 2009
dbSNP: rs13201769
rs13201769
HCG20
4 1.000 6 30788289 intron variant G/A snv 0.35 0.700 1.000 1 2010 2010
dbSNP: rs13207315
rs13207315
HLA-B ; HLA-C
4 1.000 6 31273350 intron variant T/C snv 0.13 0.700 1.000 1 2009 2009
dbSNP: rs13216197
rs13216197
HLA-B ; LINC02571 ; LOC112267902
4 1.000 6 31303241 intron variant T/C snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs13220225
rs13220225
HCG20
4 1.000 6 30780025 intron variant G/A snv 0.16 0.700 1.000 1 2010 2010
dbSNP: rs1330950
rs1330950
LINC00551
5 1.000 13 106686453 intron variant C/A snv 0.62 0.700 1.000 1 2014 2014
dbSNP: rs1349596
rs1349596
CADPS
5 1.000 3 62542448 intron variant C/T snv 6.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs143633948
rs143633948
ARG1
6 0.882 0.080 6 131504454 intron variant G/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs148332376
rs148332376
RHOH
5 1.000 4 40240870 intron variant -/T delins 7.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs1514687
rs1514687
TPO
5 1.000 2 1434216 intron variant T/G snv 0.86 0.700 1.000 1 2014 2014
dbSNP: rs16823858
rs16823858 		5 0.925 3 115559835 intron variant G/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs16897900
rs16897900
HCG20
4 1.000 6 30788116 intron variant C/A snv 0.35 0.700 1.000 1 2010 2010
dbSNP: rs16899205
rs16899205
HLA-B ; LINC02571 ; LOC112267902
4 1.000 6 31298584 intron variant A/G snv 0.34 0.700 1.000 1 2010 2010
dbSNP: rs16899207
rs16899207
HLA-B ; LINC02571 ; LOC112267902
4 1.000 6 31298610 intron variant A/G snv 0.34 0.700 1.000 1 2010 2010
dbSNP: rs16914280
rs16914280
GRM5
4 1.000 11 88588556 intron variant C/T snv 4.7E-02 0.800 1.000 1 2009 2009
dbSNP: rs16933829
rs16933829
PIK3C2A
5 0.925 11 17094129 intron variant T/C snv 6.2E-02 0.700 1.000 1 2015 2015
dbSNP: rs17038463
rs17038463
CNTN6
5 0.925 3 1383484 intron variant T/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs17079875
rs17079875
RNF130
5 1.000 5 179974542 intron variant G/A snv 6.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs17169
rs17169
LINC00298 ; LINC00299
5 0.925 2 8037334 intron variant G/T snv 0.13 0.700 1.000 1 2015 2015
dbSNP: rs17171670
rs17171670
SUGCT ; LOC105375245
5 1.000 7 40294343 intron variant T/G snv 8.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs17291045
rs17291045
LINC02477
4 1.000 4 160585745 intron variant C/T snv 9.3E-02 0.800 1.000 1 2009 2009
dbSNP: rs17481190
rs17481190
HCG20
4 1.000 6 30775237 intron variant C/T snv 0.16 0.700 1.000 1 2010 2010
dbSNP: rs17691394
rs17691394
GRM8
5 0.925 7 126684537 intron variant A/G snv 0.13 0.700 1.000 1 2010 2010
dbSNP: rs1777672
rs1777672
NBEA
4 1.000 13 35603682 intron variant G/A snv 0.94 0.800 1.000 1 2009 2009
dbSNP: rs17863787
rs17863787
UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A9
9 0.925 0.040 2 233702448 intron variant T/G snv 0.30 0.700 1.000 1 2015 2015