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: rs1015164
rs1015164
CCRL2
8 0.925 3 46410189 intron variant A/C;G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs10892324
rs10892324
SLC37A4
5 0.925 11 119032329 upstream gene variant T/A;G snv 0.700 1.000 1 2015 2015
dbSNP: rs11157436
rs11157436
TRAV30
7 0.851 0.040 14 22168978 synonymous variant C/T snv 0.19 0.700 1.000 1 2017 2017
dbSNP: rs11231017
rs11231017 		5 0.925 11 62293877 downstream gene variant G/A snv 0.29 0.700 1.000 1 2015 2015
dbSNP: rs11649112
rs11649112
SHISA9 ; LOC107984137
5 0.925 16 13267554 intron variant G/A snv 0.22 0.700 1.000 1 2015 2015
dbSNP: rs11790131
rs11790131
LOC105375988
6 0.882 0.080 9 19469848 intergenic variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs12460243
rs12460243
FBN3
5 0.925 19 8066356 intron variant G/A snv 0.14 0.700 1.000 1 2017 2017
dbSNP: rs13064773
rs13064773 		5 0.925 3 158893105 intergenic variant G/A snv 0.39 0.700 1.000 1 2015 2015
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: rs16823858
rs16823858 		5 0.925 3 115559835 intron variant G/A;C snv 0.700 1.000 1 2015 2015
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: rs17151904
rs17151904 		5 0.925 7 25568789 TF binding site variant G/A;C snv 0.700 1.000 1 2010 2010
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: rs17691394
rs17691394
GRM8
5 0.925 7 126684537 intron variant A/G snv 0.13 0.700 1.000 1 2010 2010
dbSNP: rs2229116
rs2229116
RYR3
9 0.827 0.080 15 33613209 missense variant A/G snv 0.23 0.21 0.700 1.000 1 2010 2010
dbSNP: rs2442719
rs2442719
HLA-B
6 0.882 0.120 6 31352761 intron variant C/T snv 0.53 0.700 1.000 1 2015 2015
dbSNP: rs30388
rs30388
MAF
5 0.925 16 79580219 regulatory region variant T/C;G snv 0.700 1.000 1 2015 2015
dbSNP: rs35467001
rs35467001
SDK2
6 0.882 0.080 17 73383923 missense variant G/A snv 5.3E-02 6.3E-02 0.700 1.000 1 2016 2016
dbSNP: rs35897606
rs35897606
KIAA1549L
6 0.882 0.080 11 33436311 intron variant A/G snv 4.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs4835796
rs4835796
REEP2
5 0.925 5 138446426 3 prime UTR variant T/G snv 0.56 0.700 1.000 1 2015 2015
dbSNP: rs59440261
rs59440261
MICA
5 0.925 6 31403294 intron variant C/A snv 3.3E-02 0.700 1.000 1 2015 2015
dbSNP: rs608114
rs608114
LOC107986626
5 0.925 6 95928822 intron variant A/T snv 0.95 0.700 1.000 1 2015 2015
dbSNP: rs61550741
rs61550741
TIAM1
5 0.925 21 31133966 intron variant A/G snv 0.12 0.700 1.000 1 2015 2015
dbSNP: rs6542826
rs6542826
RANBP2 ; SH3RF3
5 0.925 2 109433263 intron variant A/G snv 0.51 0.700 1.000 1 2017 2017