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: rs7750641
rs7750641
TCF19
6 0.807 0.360 6 31161533 missense variant C/T snv 7.0E-02 7.6E-02 0.700 1.000 1 2011 2011
dbSNP: rs7775397
rs7775397
TSBP1 ; TSBP1-AS1
7 0.790 0.400 6 32293475 missense variant T/G snv 6.0E-02 6.4E-02 0.700 1.000 1 2011 2011
dbSNP: rs9267522
rs9267522
PRRC2A
1 1.000 0.120 6 31635993 synonymous variant A/G snv 0.700 1.000 1 2011 2011
dbSNP: rs352139
rs352139
TLR9
18 0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 0.010 1.000 1 2013 2013
dbSNP: rs352140
rs352140
TLR9
42 0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 0.010 1.000 1 2013 2013
dbSNP: rs35771982
rs35771982
PLA2R1
2 0.925 0.120 2 160028907 missense variant G/C snv 0.39 0.35 0.010 1.000 1 2014 2014
dbSNP: rs17830558
rs17830558
PLA2R1
1 1.000 0.120 2 160021853 intron variant T/G snv 0.39 0.710 1.000 1 2017 2017
dbSNP: rs9272729
rs9272729
HLA-DQA1 ; HLA-DQA2 ; LOC107986589
1 1.000 0.120 6 32641817 intron variant G/A;C snv 0.710 1.000 1 2017 2017