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: rs741761
rs741761
SEMA7A ; MIR6881
3 0.882 0.200 15 74411588 missense variant T/A;C snv 1.8E-04; 0.35 0.010 1.000 1 2019 2019
dbSNP: rs7574865
rs7574865
STAT4
59 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2013 2013
dbSNP: rs1061622
rs1061622
TNFRSF1B
33 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1.000 1 2001 2001
dbSNP: rs10489265
rs10489265
TNFSF4 ; LOC100506023
5 0.827 0.200 1 173266926 regulatory region variant A/C snv 0.21 0.010 1.000 1 2013 2013
dbSNP: rs12720270
rs12720270
TYK2
4 0.851 0.240 19 10365084 intron variant G/A snv 0.21 0.16 0.010 1.000 1 2019 2019
dbSNP: rs12720356
rs12720356
TYK2
12 0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs2304256
rs2304256
TYK2
13 0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 0.010 1.000 1 2019 2019
dbSNP: rs280500
rs280500
TYK2
3 0.882 0.200 19 10379726 5 prime UTR variant A/G snv 0.20 0.010 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 0.010 1.000 1 2019 2019