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: rs9356744
rs9356744
7 0.882 0.120 6 20685255 intron variant T/C snv 0.42 0.700 1.000 2 2012 2014
dbSNP: rs2206734
rs2206734
6 0.882 0.160 6 20694653 intron variant C/T snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs7766070
rs7766070
3 1.000 0.080 6 20686342 intron variant C/A snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs9368219
rs9368219
3 1.000 0.080 6 20674460 intron variant C/T snv 0.19 0.700 1.000 1 2012 2012
dbSNP: rs9368222
rs9368222
8 1.000 0.080 6 20686765 intron variant C/A;T snv 0.700 1.000 1 2012 2012