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: rs80338845
rs80338845
11 0.756 0.179 11 112088971 missense variant G/T snp 0.730 1.000 3 2001 2009
dbSNP: rs80338844
rs80338844
14 0.734 0.214 11 112088939 missense variant C/T snp 2.0E-05 3.2E-05 0.720 1.000 2 2002 2006
dbSNP: rs80338847
rs80338847
7 0.784 0.179 11 112094906 missense variant T/C snp 0.710 1.000 1 2001 2001
dbSNP: rs104894304
rs104894304
8 0.784 0.179 11 112094831 missense variant A/G snp 0.700 2 2001 2004
dbSNP: rs104894302
rs104894302
10 0.756 0.179 11 112089002 missense variant A/G,T snp 4.0E-06 0.700 1 2000 2000
dbSNP: rs104894309
rs104894309
4 0.878 0.143 11 112086940 stop gained C/A,T snp 4.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs11214077
rs11214077
6 0.821 0.107 11 112087953 missense variant A/G snp 6.6E-03 4.8E-03 0.010 1.000 1 2002 2002
dbSNP: rs121913233
rs121913233
25 0.657 0.429 11 533874 missense variant T/A,C,G snp 0.010 1.000 1 2016 2016
dbSNP: rs142441643
rs142441643
6 0.821 0.179 5 223509 stop gained C/T snp 2.0E-04 3.2E-04 0.010 1.000 1 2015 2015
dbSNP: rs28933406
rs28933406
24 0.667 0.429 11 533875 missense variant G/C,T snp 0.010 1.000 1 2016 2016
dbSNP: rs34677591
rs34677591
5 0.846 0.071 11 112086941 missense variant G/A snp 7.5E-03 5.7E-03 0.010 1.000 1 2002 2002
dbSNP: rs387906780
rs387906780
2 0.923 0.036 5 251439 missense variant C/T snp 1.2E-05 0.010 1.000 1 2010 2010
dbSNP: rs764575966
rs764575966
7 0.846 0.143 1 161356832 stop gained C/T snp 3.6E-05 3.2E-05 0.010 1.000 1 2014 2014
dbSNP: rs77724903
rs77724903
RET
12 0.734 0.214 10 43118460 missense variant A/G,T snp 4.0E-06; 2.1E-03 2.6E-03 0.010 1.000 1 2006 2006