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: rs12676
rs12676
5 0.827 0.240 3 53823776 missense variant A/C;T snv 0.77 0.010 1.000 1 2006 2006
dbSNP: rs3733890
rs3733890
16 0.708 0.480 5 79126136 missense variant G/A snv 0.30 0.28 0.010 < 0.001 1 2006 2006
dbSNP: rs7946
rs7946
6 0.851 0.160 17 17506246 missense variant C/T snv 0.59 0.59 0.010 < 0.001 1 2006 2006
dbSNP: rs9001
rs9001
2 0.925 0.080 3 53823890 missense variant T/G snv 0.15 0.17 0.010 1.000 1 2006 2006