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: rs221781
rs221781 		4 0.882 7 100698285 upstream gene variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2075184
rs2075184 		14 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 0.700 1.000 1 2015 2015
dbSNP: rs391851
rs391851 		4 0.882 5 103342219 intergenic variant A/C;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1320344
rs1320344
C12orf42
4 0.882 12 103493699 intron variant A/G snv 0.64 0.700 1.000 1 2019 2019
dbSNP: rs34536443
rs34536443
TYK2
25 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs62131887
rs62131887 		14 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 0.700 1.000 1 2015 2015
dbSNP: rs10444776
rs10444776
LOC112268138
4 0.882 14 105647030 upstream gene variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1921445
rs1921445 		4 0.882 3 106229671 intergenic variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs11839053
rs11839053 		14 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 0.700 1.000 1 2015 2015
dbSNP: rs56817615
rs56817615
CLNK
4 0.882 4 10717222 intergenic variant A/G snv 0.42 0.700 1.000 1 2019 2019
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: rs28583049
rs28583049
LOC105374033
4 0.882 3 108724568 downstream gene variant T/C snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs114378220
rs114378220
CAMK4
5 0.851 0.040 5 111230662 intron variant C/T snv 4.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs7310615
rs7310615
SH2B3
12 0.882 12 111427245 intron variant C/G snv 0.67 0.700 1.000 1 2019 2019
dbSNP: rs191252491
rs191252491
ALDH2
4 0.882 12 111773070 intron variant A/T snv 7.1E-03 0.700 1.000 1 2019 2019
dbSNP: rs8061370
rs8061370
RMI2 ; LOC105371082
4 0.882 16 11364614 intron variant A/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs6679677
rs6679677
PHTF1
26 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.700 1.000 1 2015 2015
dbSNP: rs2476601
rs2476601
PTPN22 ; AP4B1-AS1
121 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.700 1.000 1 2019 2019
dbSNP: rs4246905
rs4246905
TNFSF15
16 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 0.700 1.000 1 2015 2015
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: rs1530687
rs1530687
ARHGAP31
4 0.882 3 119395668 intron variant G/A snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs13299616
rs13299616
PSMD5 ; CUTALP
4 0.882 9 120832525 intron variant T/C snv 0.50 0.700 1.000 1 2019 2019
dbSNP: rs57791671
rs57791671 		4 0.882 3 121889586 upstream gene variant T/A snv 0.38 0.700 1.000 1 2019 2019
dbSNP: rs7088058
rs7088058
PLEKHA1
5 0.851 0.040 10 122389836 intron variant C/T snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs6840978
rs6840978
IL21-AS1
10 0.776 0.160 4 122633552 intron variant C/T snv 0.16 0.700 1.000 1 2019 2019