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: rs77316810
rs77316810
RET
10 0.776 0.200 10 43113654 missense variant T/A;C;G snv 0.760 1.000 33 1994 2017
dbSNP: rs2506004
rs2506004
RET
3 0.882 0.160 10 43086825 intron variant A/C;T snv 0.050 1.000 5 2011 2015
dbSNP: rs7835688
rs7835688
2 0.925 0.080 8 32553981 intron variant G/A;C;T snv 0.050 0.800 5 2014 2019
dbSNP: rs1800858
rs1800858
RET
4 0.851 0.160 10 43100520 synonymous variant A/C;G snv 0.73 0.040 1.000 4 1999 2014
dbSNP: rs76262710
rs76262710
RET
17 0.724 0.280 10 43113648 missense variant T/A;C;G snv 4.0E-06; 4.0E-06 0.030 1.000 3 1996 1998
dbSNP: rs77503355
rs77503355
RET
8 0.776 0.160 10 43113655 missense variant G/A;C;T snv 0.730 1.000 3 1998 2009
dbSNP: rs142569954
rs142569954
3 0.882 0.160 13 77918396 missense variant C/G;T snv 4.1E-06; 2.1E-05 0.020 1.000 2 2003 2007
dbSNP: rs1800861
rs1800861
RET
3 0.882 0.160 10 43118395 synonymous variant G/A;T snv 0.74 0.020 1.000 2 1999 2014
dbSNP: rs1800863
rs1800863
RET
4 0.851 0.160 10 43120185 synonymous variant C/A;G snv 1.6E-05; 0.21 0.020 1.000 2 1999 2010
dbSNP: rs2565200
rs2565200
RET
2 0.925 0.160 10 43127485 3 prime UTR variant T/A;C snv 0.710 1.000 2 2009 2014
dbSNP: rs377767396
rs377767396
RET
2 0.925 0.080 10 43113623 missense variant C/G;T snv 0.020 0.500 2 1994 1998
dbSNP: rs74799832
rs74799832
RET
33 0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 0.020 1.000 2 1999 2009
dbSNP: rs77724903
rs77724903
RET
23 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.720 1.000 2 2009 2013
dbSNP: rs104894389
rs104894389
2 0.925 0.080 13 77901185 stop gained C/G;T snv 4.0E-06 0.010 1.000 1 1997 1997
dbSNP: rs10883866
rs10883866
3 0.882 0.160 10 81883883 intron variant C/A;G;T snv 0.010 1.000 1 2017 2017
dbSNP: rs11241200
rs11241200
MCC
1 1.000 0.080 5 113339402 intron variant T/A;G snv 0.010 1.000 1 2018 2018
dbSNP: rs11795613
rs11795613
2 0.925 0.120 X 71147478 intron variant A/G snv 0.010 1.000 1 2018 2018
dbSNP: rs12428625
rs12428625
2 0.925 0.080 13 86134644 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1421589
rs1421589
1 1.000 0.080 2 50063015 intron variant A/G;T snv 0.010 1.000 1 2018 2018
dbSNP: rs1447295
rs1447295
29 0.658 0.400 8 127472793 intron variant A/C;T snv 0.010 1.000 1 2008 2008
dbSNP: rs1799939
rs1799939
RET
27 0.658 0.280 10 43114671 missense variant G/A;C;T snv 0.21 0.010 1.000 1 1999 1999
dbSNP: rs192966556
rs192966556
1 1.000 0.080 1 228022684 missense variant C/T snv 8.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs2066845
rs2066845
46 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.010 1.000 1 2010 2010
dbSNP: rs2304678
rs2304678
1 1.000 0.080 2 27130639 stop gained G/A;C snv 4.0E-06; 0.17 0.700 1.000 1 2009 2009
dbSNP: rs2435356
rs2435356
RET
1 1.000 0.080 10 43087702 intron variant A/G;T snv 0.700 1.000 1 2009 2009