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: rs113488022
rs113488022
267 0.407 0.786 7 140753336 missense variant snp 4.0E-06 0.750 1.000 6 2004 2018
dbSNP: rs28934578
rs28934578
27 0.647 0.357 17 7675088 missense variant snp 4.0E-06 0.700 3 2000 2015
dbSNP: rs1057519757
rs1057519757
5 0.878 0.107 5 68293310 missense variant G/A,C snp 0.700 2 2010 2015
dbSNP: rs1057519823
rs1057519823
1 15 66481830 missense variant T/C snp 0.700 2 2010 2014
dbSNP: rs11540652
rs11540652
40 0.618 0.464 17 7674220 missense variant C/A,G,T snp 1.2E-05 0.700 2 2014 2015
dbSNP: rs11554273
rs11554273
19 0.707 0.214 20 58909365 missense variant C/A,G,T snp 4.0E-06 0.700 2 2012 2015
dbSNP: rs121913355
rs121913355
17 0.699 0.393 7 140781602 stop lost C/A,G,T snp 4.0E-06 0.700 2 2004 2015
dbSNP: rs121913495
rs121913495
22 0.679 0.250 20 58909366 missense variant G/A,T snp 0.700 2 2012 2015
dbSNP: rs28934575
rs28934575
25 0.673 0.321 17 7674230 missense variant C/A,G,T snp 0.700 2 2006 2015
dbSNP: rs730880502
rs730880502
1 15 66436762 missense variant T/A,G snp 0.700 2 2010 2014
dbSNP: rs773686816
rs773686816
1 5 68295271 synonymous variant C/A,G,T snp 4.0E-06 0.700 2 2014 2015
dbSNP: rs104894228
rs104894228
26 0.662 0.500 11 534286 missense variant C/A,G,T snp 0.700 1 2015 2015
dbSNP: rs1057519730
rs1057519730
2 1.000 0.036 15 66436786 missense variant T/A,G snp 0.700 1 2010 2010
dbSNP: rs1057519816
rs1057519816
9 0.801 0.214 17 39711955 missense variant C/A,T snp 0.700 1 2012 2012
dbSNP: rs1057519817
rs1057519817
1 12 56088073 missense variant C/A,G snp 4.0E-06 0.700 1 2013 2013
dbSNP: rs1057519819
rs1057519819
1 15 66436750 missense variant T/C snp 0.700 1 2010 2010
dbSNP: rs1057519820
rs1057519820
1 15 66436810 missense variant A/C snp 0.700 1 2010 2010
dbSNP: rs1057519821
rs1057519821
1 15 66436814 missense variant G/C,T snp 0.700 1 2010 2010
dbSNP: rs1057519822
rs1057519822
1 15 66481818 missense variant T/A snp 0.700 1 2010 2010
dbSNP: rs1057519824
rs1057519824
MET
2 7 116783374 missense variant T/G snp 0.700 1 2007 2007
dbSNP: rs1057519836
rs1057519836
2 3 41224630 missense variant A/C,G,T snp 0.700 1 2015 2015
dbSNP: rs1057519837
rs1057519837
2 1.000 0.036 3 41224631 missense variant C/G,T snp 0.700 1 2015 2015
dbSNP: rs1057519838
rs1057519838
1 5 68293790 stop gained C/T snp 0.700 1 2015 2015
dbSNP: rs1057519839
rs1057519839
1 5 68295257 missense variant G/T snp 0.700 1 2015 2015
dbSNP: rs1057519840
rs1057519840
1 5 68295257 inframe deletion TGACAAACGTATGAACAGC/T in-del 0.700 1 2015 2015