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: rs2104286
rs2104286
7 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.700 1.000 1 2016 2016
dbSNP: rs3118471
rs3118471
5 0.827 0.120 10 6060794 intron variant A/G snv 0.24 0.700 1.000 1 2016 2016
dbSNP: rs61839660
rs61839660
9 0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs706778
rs706778
15 0.695 0.320 10 6056986 intron variant C/T snv 0.46 0.700 1.000 1 2015 2015