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: rs12807063
rs12807063
1 11 102771779 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs17860955
rs17860955
1 11 102778751 splice acceptor variant T/C snv 1.4E-02 1.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs17860967
rs17860967
1 11 102777326 intron variant T/C snv 0.11 0.700 1.000 1 2018 2018
dbSNP: rs17878931
rs17878931
1 11 102795924 intron variant G/T snv 0.11 0.700 1.000 1 2018 2018
dbSNP: rs471994
rs471994
1 11 102827000 intron variant G/A snv 0.44 0.700 1.000 1 2018 2018
dbSNP: rs486055
rs486055
3 0.925 0.120 11 102779693 missense variant C/G;T snv 1.2E-05; 0.10 0.700 1.000 1 2018 2018
dbSNP: rs575027
rs575027
1 11 102837183 intron variant A/G snv 0.54 0.700 1.000 1 2018 2018