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 0.020 1.000 2 2003 2017
dbSNP: rs121913529
rs121913529
70 0.559 0.393 12 25245350 missense variant C/A,G,T snp 4.0E-06 0.020 1.000 2 2010 2015
dbSNP: rs11191439
rs11191439
4 0.923 0.107 10 102878966 missense variant T/A,C snp 9.2E-02 9.8E-02 0.010 1.000 1 2009 2009
dbSNP: rs16906252
rs16906252
9 0.821 0.107 10 129467281 synonymous variant C/T snp 5.5E-02 5.9E-02 0.010 1.000 1 2011 2011
dbSNP: rs61748181
rs61748181
5 0.923 0.071 5 1294051 missense variant C/T snp 2.2E-02 2.8E-02 0.010 1.000 1 2015 2015
dbSNP: rs752021744
rs752021744
21 0.699 0.429 3 138759306 T/C snp 1.2E-05 0.010 1.000 1 2015 2015
dbSNP: rs759728549
rs759728549
26 0.679 0.214 17 7676223 stop lost T/C snp 8.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs796065354
rs796065354
9 0.801 0.107 6 151944320 missense variant A/G snp 0.010 1.000 1 2009 2009
dbSNP: rs79658334
rs79658334
RET
19 0.685 0.321 10 43119548 missense variant G/A,C,T snp 1.2E-04; 4.3E-06 2.2E-04 0.010 1.000 1 2008 2008