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: rs9400239
rs9400239
3 1.000 6 108656460 5 prime UTR variant T/C snv 0.55 0.700 1.000 3 2015 2018
dbSNP: rs3800229
rs3800229
4 1.000 0.040 6 108675760 intron variant G/T snv 0.54 0.700 1.000 2 2017 2017
dbSNP: rs12206094
rs12206094
2 6 108584997 intron variant C/T snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs2253310
rs2253310
1 6 108567390 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs3800230
rs3800230
1 6 108676925 intron variant T/G snv 0.15 0.700 1.000 1 2019 2019