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: rs79658334
rs79658334
RET
29 0.662 0.360 10 43119548 missense variant G/A;C;T snv 1.2E-04; 4.3E-06 0.880 1.000 16 1996 2018
dbSNP: rs76262710
rs76262710
RET
17 0.724 0.280 10 43113648 missense variant T/A;C;G snv 4.0E-06; 4.0E-06 0.870 1.000 34 1993 2018
dbSNP: rs75234356
rs75234356
RET
14 0.716 0.240 10 43120144 missense variant T/G snv 1.2E-05 7.0E-06 0.870 1.000 27 1993 2018
dbSNP: rs79781594
rs79781594
RET
16 0.732 0.160 10 43113649 missense variant G/A;C;T snv 0.830 1.000 31 1993 2018
dbSNP: rs78014899
rs78014899
RET
12 0.742 0.160 10 43118392 missense variant G/A;C;T snv 8.0E-06 0.830 1.000 11 1996 2018
dbSNP: rs75030001
rs75030001
RET
7 0.807 0.160 10 43118458 missense variant G/C;T snv 4.0E-06; 2.0E-05 0.830 1.000 3 2012 2018
dbSNP: rs75996173
rs75996173
RET
21 0.716 0.240 10 43114501 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 0.820 1.000 30 1993 2018
dbSNP: rs77724903
rs77724903
RET
23 0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 0.810 1.000 21 1993 2007
dbSNP: rs77503355
rs77503355
RET
8 0.776 0.160 10 43113655 missense variant G/A;C;T snv 0.800 1.000 8 1996 2017
dbSNP: rs77939446
rs77939446
RET
15 0.724 0.120 10 43113622 missense variant G/A;C;T snv 4.0E-06 0.800 1.000 8 1996 2017
dbSNP: rs74799832
rs74799832
RET
33 0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 0.770 1.000 7 1996 2018
dbSNP: rs75076352
rs75076352
RET
24 0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05 0.740 1.000 4 1994 2018
dbSNP: rs75873440
rs75873440
RET
10 0.763 0.200 10 43112173 missense variant G/A;T snv 4.4E-05 0.730 1.000 3 2003 2008
dbSNP: rs77316810
rs77316810
RET
10 0.776 0.200 10 43113654 missense variant T/A;C;G snv 0.730 1.000 3 1994 2018
dbSNP: rs77709286
rs77709286
RET
12 0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 0.710 1.000 21 1993 2004
dbSNP: rs55947360
rs55947360
RET
1 1.000 0.120 10 43119669 missense variant G/A;T snv 4.0E-05; 4.0E-06 0.700 1.000 20 1993 2001
dbSNP: rs80069458
rs80069458
RET
3 0.882 0.120 10 43113629 missense variant C/G;T snv 0.700 1.000 20 1993 2001
dbSNP: rs377767434
rs377767434
RET
1 1.000 0.120 10 43112153 protein altering variant -/AGGAGTGTG delins 0.700 1.000 1 1999 1999
dbSNP: rs377767391
rs377767391
RET
5 0.827 0.160 10 43113627 missense variant T/A;C;G snv 0.700 0
dbSNP: rs377767405
rs377767405
RET
5 0.827 0.120 10 43114489 missense variant G/A;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: rs377767432
rs377767432
RET
2 0.925 0.160 10 43121980 missense variant C/A;T snv 0.700 0
dbSNP: rs543320028
rs543320028
NTRK1
2 0.925 0.160 1 156864394 missense variant C/A;T snv 4.0E-06; 1.2E-05 0.700 0
dbSNP: rs77558292
rs77558292
RET
8 0.776 0.160 10 43113621 missense variant T/A;C;G snv 0.700 0
dbSNP: rs78347871
rs78347871
RET
3 0.882 0.120 10 43121950 missense variant G/A;C;T snv 8.0E-06; 2.0E-05 0.700 0