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: rs104893875
rs104893875
11 0.756 0.107 4 89828170 missense variant C/T snp 4.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs104893877
rs104893877
31 0.679 0.250 4 89828149 missense variant C/T snp 0.010 1.000 1 2001 2001
dbSNP: rs201106962
rs201106962
8 0.784 0.143 4 89828156 missense variant A/C snp 8.0E-05 9.6E-05 0.010 1.000 1 2014 2014