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: rs77316810
rs77316810
RET
10 0.776 0.200 10 43113654 missense variant T/A;C;G snv 0.720 1.000 40 1993 2017
dbSNP: rs79781594
rs79781594
RET
16 0.732 0.160 10 43113649 missense variant G/A;C;T snv 0.710 1.000 26 1993 2016
dbSNP: rs77503355
rs77503355
RET
8 0.776 0.160 10 43113655 missense variant G/A;C;T snv 0.710 1.000 19 1993 2011
dbSNP: rs377767397
rs377767397
RET
10 0.790 0.280 10 43113628 missense variant G/A;C;T snv 0.700 1.000 13 1994 2018
dbSNP: rs377767405
rs377767405
RET
5 0.827 0.120 10 43114489 missense variant G/A;C;T snv 0.700 1.000 11 1995 2015
dbSNP: rs377767442
rs377767442
RET
5 0.827 0.160 10 43121967 missense variant A/G snv 0.700 1.000 11 1994 2019
dbSNP: rs77558292
rs77558292
RET
8 0.776 0.160 10 43113621 missense variant T/A;C;G snv 0.700 1.000 9 1996 2011
dbSNP: rs377767391
rs377767391
RET
5 0.827 0.160 10 43113627 missense variant T/A;C;G snv 0.700 1.000 8 1996 2009
dbSNP: rs377767404
rs377767404
RET
11 0.742 0.160 10 43114488 missense variant T/C snv 0.700 1.000 8 1997 2015
dbSNP: rs80069458
rs80069458
RET
3 0.882 0.120 10 43113629 missense variant C/G;T snv 0.700 1.000 6 1993 2011
dbSNP: rs377767398
rs377767398
RET
8 0.807 0.280 10 43113628 missense variant GC/AT;CT;TT mnv 0.700 1.000 5 1999 2011
dbSNP: rs377767408
rs377767408
RET
1 1.000 0.120 10 43114496 missense variant GCTGT/CGTGC mnv 0.700 1.000 3 1993 1996
dbSNP: rs377767440
rs377767440
RET
1 1.000 0.120 10 43114598 protein altering variant G/TTCT delins 0.700 1.000 3 2005 2017
dbSNP: rs267607011
rs267607011
RET
2 1.000 0.120 10 43120184 missense variant C/G;T snv 0.700 1.000 2 2007 2011
dbSNP: rs377767400
rs377767400
RET
1 1.000 0.120 10 43113650 missense variant C/G;T snv 0.700 1.000 2 1998 2004
dbSNP: rs1554818626
rs1554818626
RET
1 1.000 0.120 10 43112121 missense variant C/G snv 0.700 1.000 1 2015 2015
dbSNP: rs377767389
rs377767389
RET
1 1.000 0.120 10 43112120 missense variant GC/CT mnv 0.700 1.000 1 2008 2008
dbSNP: rs377767438
rs377767438
RET
1 1.000 0.120 10 43114506 protein altering variant A/GACCTGTGCCGCC delins 0.700 1.000 1 2005 2005
dbSNP: rs1060500759
rs1060500759
RET
1 1.000 0.120 10 43120162 stop gained C/T snv 0.700 0
dbSNP: rs377767412
rs377767412
RET
7 0.790 0.240 10 43114547 synonymous variant G/A snv 0.700 0
dbSNP: rs74799832
rs74799832
RET
33 0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 0.700 1.000 8 1994 2016
dbSNP: rs75030001
rs75030001
RET
7 0.807 0.160 10 43118458 missense variant G/C;T snv 4.0E-06; 2.0E-05 0.700 1.000 12 1998 2013
dbSNP: rs77724903
rs77724903
RET
23 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.010 < 0.001 1 2013 2013
dbSNP: rs146838520
rs146838520
RET
4 0.851 0.120 10 43120129 missense variant C/T snv 4.0E-06 2.8E-05 0.010 1.000 1 2006 2006
dbSNP: rs76262710
rs76262710
RET
17 0.724 0.280 10 43113648 missense variant T/A;C;G snv 4.0E-06; 4.0E-06 0.720 1.000 35 1993 2016