Source: ALL
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: rs398122820
rs398122820
B2M
8 0.790 0.240 15 44715641 missense variant G/A snv 0.050 1.000 5 2012 2019
dbSNP: rs387906535
rs387906535
LYZ
2 0.925 0.080 12 69350170 missense variant G/C snv 7.0E-06 0.020 1.000 2 2004 2008
dbSNP: rs121909612
rs121909612
FGA
6 0.807 0.160 4 154585795 missense variant T/A snv 4.0E-06 7.0E-06 0.010 1.000 1 2000 2000
dbSNP: rs121913547
rs121913547
LYZ
7 0.807 0.200 12 69350192 missense variant T/C snv 0.010 1.000 1 2004 2004
dbSNP: rs1800973
rs1800973
LYZ
9 0.827 0.320 12 69350234 missense variant C/A snv 4.2E-02 4.3E-02 0.010 1.000 1 2008 2008
dbSNP: rs730881163
rs730881163
TTR
3 0.882 0.160 18 31595155 missense variant C/A snv 0.010 1.000 1 1995 1995