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: rs10812774
rs10812774
2 0.925 0.040 9 28294233 intron variant T/C snv 0.49 0.010 1.000 1 2011 2011
dbSNP: rs7033345
rs7033345
3 0.882 0.080 9 28717575 intergenic variant T/C;G snv 0.35 0.010 1.000 1 2011 2011