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: rs9276370
rs9276370
3 0.882 0.200 6 32739518 upstream gene variant G/T snv 0.51 0.710 1.000 2 2011 2014
dbSNP: rs2051598
rs2051598
1 1.000 0.080 6 32741586 intron variant G/A snv 0.71 0.700 1.000 1 2013 2013
dbSNP: rs2213565
rs2213565
1 1.000 0.080 6 32745411 splice region variant C/T snv 0.81 0.80 0.700 1.000 1 2013 2013
dbSNP: rs9276394
rs9276394
2 0.925 0.200 6 32740690 upstream gene variant T/A snv 0.80 0.700 1.000 1 2013 2013
dbSNP: rs9276395
rs9276395
2 0.925 0.200 6 32740727 upstream gene variant C/A;G snv 0.700 1.000 1 2013 2013
dbSNP: rs9276396
rs9276396
1 1.000 0.080 6 32740959 upstream gene variant T/C snv 0.80 0.700 1.000 1 2013 2013
dbSNP: rs9276427
rs9276427
2 0.925 0.120 6 32744080 intron variant T/C snv 0.57 0.700 1.000 1 2013 2013