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: rs7025694
rs7025694
TRPM3 ; LOC101927086
1 1.000 0.240 9 70550347 intron variant T/C snv 0.48 0.010 < 0.001 1 2016 2016
dbSNP: rs7216389
rs7216389
GSDMB
14 0.732 0.440 17 39913696 intron variant C/T snv 0.60 0.010 1.000 1 2017 2017
dbSNP: rs7615856
rs7615856
DCBLD2
1 1.000 0.240 3 98869133 intron variant C/T snv 0.36 0.010 1.000 1 2012 2012
dbSNP: rs828621
rs828621
DCBLD2
1 1.000 0.240 3 98824818 intron variant T/A snv 0.35 0.010 1.000 1 2012 2012
dbSNP: rs870830
rs870830
GSDMB
1 1.000 0.240 17 39912120 intron variant G/A;C snv 0.010 1.000 1 2017 2017
dbSNP: rs8833
rs8833
ST3GAL6 ; DCBLD2
1 1.000 0.240 3 98796725 3 prime UTR variant C/T snv 0.30 0.010 1.000 1 2012 2012
dbSNP: rs9268644
rs9268644
HLA-DRA
5 0.827 0.360 6 32440267 intron variant A/C snv 0.68 0.010 1.000 1 2012 2012