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: rs6010620
rs6010620
3 0.701 0.360 20 63678486 intron variant A/C;G snv 0.810 0.667 1 2011 2015
dbSNP: rs4809219
rs4809219
1 1.000 0.120 20 63671762 intron variant C/A;G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs909341
rs909341
1 1.000 0.120 20 63697389 synonymous variant C/T snv 0.25 0.19 0.700 1.000 1 2015 2015