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: rs9357271
rs9357271
8 0.776 0.160 6 38398097 intron variant T/C snv 0.38 0.880 1.000 11 2007 2019
dbSNP: rs3923809
rs3923809
1 1.000 0.080 6 38473194 intron variant A/G snv 0.32 0.820 1.000 4 2007 2017
dbSNP: rs9296249
rs9296249
3 0.882 0.120 6 38398065 intron variant T/C snv 0.30 0.820 1.000 3 2007 2017
dbSNP: rs4236060
rs4236060
1 1.000 0.080 6 38502311 intron variant C/T snv 0.22 0.700 1.000 1 2007 2007
dbSNP: rs4714156
rs4714156
2 0.925 0.120 6 38393336 intron variant C/T snv 0.36 0.700 1.000 1 2007 2007
dbSNP: rs61192259
rs61192259
1 1.000 0.080 6 38486186 intron variant C/A snv 0.50 0.700 1.000 1 2017 2017
dbSNP: rs6904723
rs6904723
1 1.000 0.080 6 38468541 intron variant A/C;T snv 0.700 1.000 1 2007 2007
dbSNP: rs6923737
rs6923737
1 1.000 0.080 6 38515788 intron variant T/C snv 0.28 0.700 1.000 1 2007 2007