Source: BEFREE ×
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: rs3806932
rs3806932
TSLP
2 0.925 0.160 5 111069977 upstream gene variant A/G snv 0.51 0.720 1.000 2 2010 2015
dbSNP: rs10062929
rs10062929
TSLP
1 1.000 0.120 5 111072481 intron variant C/A snv 0.13 0.010 1.000 1 2010 2010
dbSNP: rs1059513
rs1059513
NAB2 ; STAT6
4 0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 0.010 1.000 1 2019 2019
dbSNP: rs2416257
rs2416257
WDR36
4 0.882 0.160 5 111099792 intron variant C/G;T snv 0.010 1.000 1 2015 2015
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: rs4671393
rs4671393
BCL11A
9 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: 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: rs7482144
rs7482144
HBG2
3 0.882 0.280 11 5254939 3 prime UTR variant G/A snv 0.010 1.000 1 2015 2015
dbSNP: rs9399137
rs9399137
HBS1L
5 0.851 0.320 6 135097880 intron variant T/C snv 0.20 0.010 1.000 1 2015 2015