Gene: RET ×
Source: ALL
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: rs1183365192
rs1183365192
RET
4 0.851 0.160 10 43106550 missense variant C/T snv 7.0E-06 0.010 1.000 1 1997 1997
dbSNP: rs148935214
rs148935214
RET
3 0.882 0.240 10 43114546 missense variant C/T snv 3.2E-04 3.8E-04 0.010 1.000 1 2009 2009
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: rs1800860
rs1800860
RET
3 0.882 0.080 10 43111239 missense variant A/G snv 0.70 0.74 0.010 1.000 1 2010 2010
dbSNP: rs1800862
rs1800862
RET
2 0.925 0.160 10 43119646 synonymous variant C/T snv 4.5E-02 3.9E-02 0.010 1.000 1 2002 2002
dbSNP: rs1864410
rs1864410
RET
1 1.000 0.080 10 43080177 intron variant T/G snv 0.80 0.010 1.000 1 2014 2014
dbSNP: rs2075912
rs2075912
RET
2 0.925 0.160 10 43126769 3 prime UTR variant T/C snv 0.79 0.84 0.010 1.000 1 2010 2010
dbSNP: rs377767397
rs377767397
RET
10 0.790 0.280 10 43113628 missense variant G/A;C;T snv 0.010 1.000 1 2003 2003
dbSNP: rs377767398
rs377767398
RET
8 0.807 0.280 10 43113628 missense variant GC/AT;CT;TT mnv 0.010 1.000 1 2003 2003
dbSNP: rs377767432
rs377767432
RET
2 0.925 0.160 10 43121980 missense variant C/A;T snv 0.010 1.000 1 2017 2017
dbSNP: rs781362020
rs781362020
RET
1 1.000 0.080 10 43109108 missense variant T/C snv 2.8E-05 7.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs79890926
rs79890926
RET
6 0.827 0.160 10 43113656 missense variant C/G;T snv 1.6E-05 0.010 1.000 1 2007 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: rs199529397
rs199529397
RET
2 0.925 0.080 10 43109070 missense variant G/A snv 5.6E-05 6.3E-05 0.020 1.000 2 2010 2016
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: rs76397662
rs76397662
RET
4 0.851 0.200 10 43102345 missense variant G/A snv 7.9E-04 2.9E-04 0.020 1.000 2 2010 2016
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: 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: rs2506004
rs2506004
RET
3 0.882 0.160 10 43086825 intron variant A/C;T snv 0.050 1.000 5 2011 2015
dbSNP: rs1864400
rs1864400
RET
2 0.925 0.080 10 43114918 intron variant G/A;T snv 0.83 0.700 1.000 1 2014 2014
dbSNP: rs1864403
rs1864403
RET
1 1.000 0.080 10 43109502 intron variant A/G snv 0.79 0.700 1.000 1 2009 2009
dbSNP: rs2435342
rs2435342
RET
1 1.000 0.080 10 43088808 intron variant T/C snv 0.43 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