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: rs1012841819
rs1012841819
4 0.882 0.160 2 96115728 missense variant G/A snv 4.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs1024323
rs1024323
4 0.882 0.160 4 3004316 missense variant C/A;G;T snv 0.36 0.010 1.000 1 2009 2009
dbSNP: rs1334899057
rs1334899057
4 0.882 0.160 20 23035908 missense variant T/C snv 7.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs1462059537
rs1462059537
4 0.882 0.160 4 147535944 missense variant C/T snv 8.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs1801131
rs1801131
93 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2012 2012
dbSNP: rs1801133
rs1801133
174 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.010 1.000 1 2012 2012
dbSNP: rs2296545
rs2296545
8 0.851 0.160 10 88583080 missense variant C/G;T snv 0.46 0.010 1.000 1 2015 2015
dbSNP: rs397507444
rs397507444
306 0.405 0.880 1 11794407 missense variant T/G snv 0.010 1.000 1 2012 2012
dbSNP: rs758801521
rs758801521
4 0.882 0.160 8 26770618 missense variant A/G snv 4.0E-06 0.010 1.000 1 2009 2009