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: rs2303369
rs2303369
3 0.925 0.120 2 27492549 intron variant C/T snv 0.38 0.700 1.000 2 2010 2013
dbSNP: rs704795
rs704795
3 0.925 0.120 2 27493627 intron variant G/A snv 0.46 0.700 1.000 2 2010 2013
dbSNP: rs780090
rs780090
4 0.925 0.120 2 27495607 upstream gene variant T/C;G snv 0.700 1.000 1 2013 2013
dbSNP: rs8395
rs8395
2 0.925 0.120 2 27492340 3 prime UTR variant T/A snv 0.42 0.700 1.000 1 2013 2013