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: rs104893967
rs104893967
5 0.827 0.080 6 42178374 missense variant A/G snv 0.030 1.000 3 1998 2000
dbSNP: rs104893968
rs104893968
8 0.790 0.200 6 42173762 missense variant C/G;T snv 4.0E-06; 1.2E-03 0.020 1.000 2 2000 2004
dbSNP: rs121434631
rs121434631
6 0.807 0.080 6 42179248 missense variant C/G;T snv 4.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs746726029
rs746726029
1 1.000 0.040 2 232407646 missense variant A/G snv 8.0E-06 0.010 1.000 1 2000 2000
dbSNP: rs774437307
rs774437307
MPST ; TST
1 1.000 0.040 22 37018437 missense variant T/C snv 8.0E-06 0.010 1.000 1 1998 1998
dbSNP: rs930876036
rs930876036
1 1.000 0.040 1 1223249 missense variant T/C snv 4.0E-06 0.010 1.000 1 2001 2001