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 0.700 0
dbSNP: rs104893877
rs104893877
31 0.679 0.250 4 89828149 missense variant C/T snp 0.010 1.000 1 2000 2000
dbSNP: rs104893878
rs104893878
17 0.744 0.179 4 89835580 missense variant C/G snp 0.010 1.000 1 2000 2000