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: rs16884688
rs16884688
2 6 21220145 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs6939250
rs6939250
2 6 20939503 intron variant T/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs9465848
rs9465848
4 6 20635589 intron variant C/T snv 9.3E-03 0.700 1.000 1 2012 2012