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: rs3761781
rs3761781
3 6 41777210 intron variant G/A snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs6905726
rs6905726
2 6 41783074 intron variant T/C snv 0.56 0.700 1.000 1 2009 2009
dbSNP: rs6925777
rs6925777
2 6 41783084 intron variant C/T snv 0.51 0.700 1.000 1 2009 2009
dbSNP: rs9394831
rs9394831
2 6 41785346 synonymous variant C/T snv 0.21 0.19 0.700 1.000 1 2009 2009