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: rs870142
rs870142
7 0.851 0.120 4 4646320 intron variant C/G;T snv 0.020 1.000 2 2014 2016
dbSNP: rs121918460
rs121918460
27 0.708 0.400 12 112450364 missense variant T/A;G snv 4.0E-06 0.700 1.000 1 2018 2018
dbSNP: rs1555223259
rs1555223259
3 1.000 0.080 12 114355868 stop gained G/C snv 0.700 1.000 1 2018 2018
dbSNP: rs899127658
rs899127658
F2
82 0.547 0.720 11 46739084 missense variant G/A;C snv 0.010 1.000 1 2012 2012
dbSNP: rs1057518422
rs1057518422
7 0.851 0.240 6 149378954 stop gained C/T snv 0.700 0
dbSNP: rs1282433424
rs1282433424
2 0.925 0.080 8 11755094 missense variant C/T snv 0.700 0
dbSNP: rs1217691063
rs1217691063
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs3729856
rs3729856
3 0.925 0.080 8 11757066 missense variant A/G snv 9.5E-02 9.0E-02 0.010 1.000 1 2011 2011
dbSNP: rs16835979
rs16835979
6 0.851 0.120 4 4633549 intron variant C/A snv 0.20 0.020 1.000 2 2014 2016
dbSNP: rs6824295
rs6824295
6 0.851 0.120 4 4612553 intron variant C/T snv 0.20 0.020 1.000 2 2014 2016