Gene: RET ×
Source: CLINVAR ×
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: rs79658334
rs79658334
RET
14 0.662 0.360 10 43119548 missense variant G/A;C;T snv 1.2E-04; 4.3E-06 0.700 1.000 19 1995 2016
dbSNP: rs75030001
rs75030001
RET
4 0.807 0.160 10 43118458 missense variant G/C;T snv 4.0E-06; 2.0E-05 0.700 1.000 16 1998 2018
dbSNP: rs79781594
rs79781594
RET
8 0.732 0.160 10 43113649 missense variant G/A;C;T snv 0.700 1.000 12 1996 2015
dbSNP: rs146646971
rs146646971
RET
3 0.807 0.120 10 43114598 missense variant G/C;T snv 2.4E-05 0.700 1.000 11 2005 2016
dbSNP: rs75076352
rs75076352
RET
9 0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05 0.700 1.000 11 1994 2017
dbSNP: rs75996173
rs75996173
RET
10 0.716 0.240 10 43114501 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 0.700 1.000 9 1994 2017
dbSNP: rs76262710
rs76262710
RET
11 0.724 0.280 10 43113648 missense variant T/A;C;G snv 4.0E-06; 4.0E-06 0.700 1.000 8 1994 2015
dbSNP: rs77316810
rs77316810
RET
4 0.776 0.200 10 43113654 missense variant T/A;C;G snv 0.700 1.000 8 1994 2015
dbSNP: rs377767406
rs377767406
RET
2 0.776 0.120 10 43114491 missense variant G/A;T snv 4.0E-05; 4.0E-06 0.700 1.000 7 1995 2012
dbSNP: rs77939446
rs77939446
RET
9 0.724 0.120 10 43113622 missense variant G/A;C;T snv 4.0E-06 0.700 1.000 7 1994 2016
dbSNP: rs79890926
rs79890926
RET
3 0.827 0.160 10 43113656 missense variant C/G;T snv 1.6E-05 0.700 1.000 7 1997 2015
dbSNP: rs377767397
rs377767397
RET
2 0.790 0.280 10 43113628 missense variant G/A;C;T snv 0.700 1.000 6 1996 2017
dbSNP: rs143795581
rs143795581
RET
3 0.851 0.120 10 43114596 missense variant A/C;G snv 8.0E-06 0.700 1.000 3 2005 2015