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: rs6503525
rs6503525
LRRC3C
2 0.925 0.080 17 39938921 intron variant G/A;C snv 0.700 1.000 1 2007 2007
dbSNP: rs6503526
rs6503526
GSDMA
2 0.925 0.080 17 39958345 intron variant C/T snv 0.41 0.700 1.000 1 2007 2007
dbSNP: rs6716266
rs6716266
ANTXR1
1 1.000 0.080 2 69018096 intron variant T/G snv 0.23 0.700 1.000 1 2007 2007
dbSNP: rs7209742
rs7209742 		1 1.000 0.080 17 39952455 upstream gene variant A/G snv 0.69 0.700 1.000 1 2007 2007
dbSNP: rs7218742
rs7218742
GSDMA
1 1.000 0.080 17 39958108 intron variant A/G snv 0.70 0.700 1.000 1 2007 2007
dbSNP: rs7219923
rs7219923
GSDMB
4 0.882 0.160 17 39918265 non coding transcript exon variant C/T snv 0.52 0.700 1.000 1 2007 2007
dbSNP: rs8065126
rs8065126
LRRC3C
2 1.000 0.080 17 39942782 intron variant T/A;C snv 0.700 1.000 1 2007 2007
dbSNP: rs8067378
rs8067378 		12 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 0.700 1.000 1 2007 2007
dbSNP: rs8076131
rs8076131
ORMDL3
11 0.790 0.200 17 39924659 intron variant G/A;C snv 0.700 1.000 1 2007 2007
dbSNP: rs8076474
rs8076474
GSDMA
1 1.000 0.080 17 39954981 intron variant G/C snv 0.69 0.700 1.000 1 2007 2007
dbSNP: rs8079416
rs8079416
LRRC3C
2 0.925 0.080 17 39936460 intron variant T/C snv 0.45 0.700 1.000 1 2007 2007
dbSNP: rs8179521
rs8179521
MAP3K2-DT
1 1.000 0.080 2 127393348 intron variant A/C;G snv 0.700 1.000 1 2007 2007
dbSNP: rs907092
rs907092
IKZF3
3 0.925 0.080 17 39766006 synonymous variant G/A snv 0.41 0.36 0.700 1.000 1 2007 2007
dbSNP: rs9303277
rs9303277
IKZF3
9 0.790 0.240 17 39820216 intron variant C/T snv 0.52 0.700 1.000 1 2007 2007
dbSNP: rs9303281
rs9303281
GSDMB
4 0.882 0.160 17 39917793 non coding transcript exon variant G/A snv 0.50 0.700 1.000 1 2007 2007
dbSNP: rs7216389
rs7216389
GSDMB
14 0.732 0.440 17 39913696 intron variant C/T snv 0.60 0.080 1.000 8 2008 2018
dbSNP: rs7793837
rs7793837
CRHR2
1 1.000 0.080 7 30687161 intron variant A/C;T snv 0.010 1.000 1 2008 2008
dbSNP: rs569108
rs569108
MS4A2
8 0.790 0.200 11 60095631 missense variant A/G snv 4.7E-02 7.3E-02 0.020 1.000 2 2009 2016
dbSNP: rs1220579705
rs1220579705
IL4
1 1.000 0.080 5 132674079 missense variant C/T snv 0.010 1.000 1 2009 2009
dbSNP: rs1800470
rs1800470
TGFB1
107 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 1.000 1 2009 2009
dbSNP: rs1800471
rs1800471
TGFB1
48 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2009 2009
dbSNP: rs1805011
rs1805011
IL4R
8 0.776 0.320 16 27362551 missense variant A/C;G;T snv 0.13; 1.2E-04; 3.6E-05 0.010 1.000 1 2009 2009
dbSNP: rs2378383
rs2378383 		1 1.000 0.080 9 79424447 intergenic variant A/C;G;T snv 0.810 1.000 1 2009 2009
dbSNP: rs571448378
rs571448378
FDXR
5 0.882 0.120 17 74872110 stop gained G/A;C snv 4.1E-06; 4.1E-06 1.4E-05 0.010 1.000 1 2009 2009
dbSNP: rs748245223
rs748245223
IL4R
2 0.925 0.080 16 27363275 synonymous variant C/T snv 4.1E-06 0.010 1.000 1 2009 2009