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: rs8041227
rs8041227 		1 1.000 0.120 15 31246339 intergenic variant G/A snv 0.18 0.700 1.000 1 2014 2014
dbSNP: rs9956738
rs9956738
DCC
1 1.000 0.120 18 52414603 intron variant A/G snv 4.6E-02 0.700 1.000 1 2014 2014
dbSNP: rs3806932
rs3806932
TSLP
3 0.925 0.160 5 111069977 upstream gene variant A/G snv 0.51 0.720 1.000 2 2010 2015
dbSNP: rs2416257
rs2416257
WDR36
5 0.882 0.160 5 111099792 intron variant C/G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs4671393
rs4671393
BCL11A
11 0.790 0.400 2 60493816 intron variant A/C;G snv 0.010 1.000 1 2015 2015
dbSNP: rs489441
rs489441
C5orf66
2 0.925 0.280 5 135158291 intron variant G/A;C;T snv 0.010 1.000 1 2015 2015
dbSNP: rs7482144
rs7482144
HBG2
4 0.882 0.280 11 5254939 3 prime UTR variant G/A snv 0.010 1.000 1 2015 2015
dbSNP: rs9399137
rs9399137
HBS1L
13 0.851 0.320 6 135097880 intron variant T/C snv 0.20 0.010 1.000 1 2015 2015
dbSNP: rs6736278
rs6736278
CAPN14
1 1.000 0.120 2 31220009 intron variant C/T snv 5.4E-02 0.010 1.000 1 2018 2018
dbSNP: rs1059513
rs1059513
NAB2 ; STAT6
11 0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 0.010 1.000 1 2019 2019
dbSNP: rs11495981
rs11495981
JAZF1
2 1.000 0.120 7 28137682 intron variant C/T snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs12924112
rs12924112
CLEC16A
1 1.000 0.120 16 11125863 intron variant T/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs324011
rs324011
STAT6
12 0.742 0.360 12 57108399 intron variant C/T snv 0.32 0.010 1.000 1 2019 2019
dbSNP: rs4240384
rs4240384
LINC02240 ; LOC107986391
1 1.000 0.120 5 124955709 intron variant T/C snv 0.85 0.700 1.000 1 2019 2019
dbSNP: rs599707
rs599707 		2 0.925 0.200 6 31840659 downstream gene variant C/T snv 7.6E-02 0.700 1.000 1 2019 2019