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: rs1564489315
rs1564489315
RET
1 1.000 0.080 10 43100496 stop gained G/A snv 0.700 0
dbSNP: rs1564490097
rs1564490097
RET
1 1.000 0.080 10 43102444 missense variant T/C snv 0.700 0
dbSNP: rs1564491460
rs1564491460
RET
1 1.000 0.080 10 43105186 missense variant G/A snv 0.700 0
dbSNP: rs1564500612
rs1564500612
RET
1 1.000 0.080 10 43123732 frameshift variant -/T delins 0.700 0
dbSNP: rs1564501934
rs1564501934
RET
1 1.000 0.080 10 43126678 frameshift variant T/- del 0.700 0
dbSNP: rs193922699
rs193922699
RET
1 1.000 0.080 10 43114478 splice acceptor variant A/G snv 0.700 0
dbSNP: rs751572082
rs751572082
RET
1 1.000 0.080 10 43102608 missense variant G/A;C snv 4.8E-05 6.3E-05 0.700 0
dbSNP: rs76764689
rs76764689
RET
2 0.925 0.080 10 43100480 missense variant C/T snv 0.700 0
dbSNP: rs779996040
rs779996040
RET
1 1.000 0.080 10 43119575 missense variant C/T snv 8.3E-06 0.700 0
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: 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: rs377767396
rs377767396
RET
2 0.925 0.080 10 43113623 missense variant C/G;T snv 0.020 0.500 2 1994 1998
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: 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: rs377767391
rs377767391
RET
5 0.827 0.160 10 43113627 missense variant T/A;C;G snv 0.710 1.000 1 2003 2003
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: 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: 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: 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: 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: 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
dbSNP: rs2505533
rs2505533
RET
1 1.000 0.080 10 43099005 intron variant T/A;C snv 0.700 1.000 1 2009 2009