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: rs6946509
rs6946509
6 0.807 0.120 7 22769871 downstream gene variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs7069750
rs7069750
FAS
6 0.807 0.120 10 89002619 non coding transcript exon variant G/C;T snv 0.50 0.700 1.000 1 2013 2013
dbSNP: rs7127214
rs7127214
6 0.807 0.120 11 36322143 intron variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs7137828
rs7137828
15 0.763 0.200 12 111494996 intron variant C/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs71624119
rs71624119
8 0.776 0.200 5 56144903 intron variant G/A snv 0.17 0.700 1.000 1 2013 2013
dbSNP: rs72698115
rs72698115
6 0.807 0.120 1 154406893 intron variant A/C snv 7.2E-02 0.700 1.000 1 2013 2013
dbSNP: rs73300638
rs73300638
6 0.807 0.120 7 28147725 intron variant A/C;G snv 0.700 1.000 1 2013 2013
dbSNP: rs8129030
rs8129030
7 0.807 0.120 21 35340290 intron variant T/A;G snv 0.72 0.700 1.000 1 2013 2013
dbSNP: rs9532434
rs9532434
8 0.807 0.120 13 39781776 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs11893432
rs11893432
5 0.827 0.120 2 191057148 intron variant C/G snv 0.21 0.010 1.000 1 2019 2019