Source: CURATED ×
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: rs1483605155
rs1483605155
RET
1 1.000 10 43113579 missense variant G/A;C snv 4.1E-06 0.700 1.000 15 1994 2011
dbSNP: rs1554818362
rs1554818362
RET
2 1.000 10 43109163 missense variant C/T snv 0.800 1.000 15 1994 2011
dbSNP: rs183729115
rs183729115
RET
1 1.000 10 43109156 missense variant G/A snv 0.700 1.000 15 1994 2011
dbSNP: rs536486113
rs536486113
RET
1 1.000 10 43126717 missense variant T/A;C snv 4.0E-06; 4.0E-06 0.700 1.000 15 1994 2011
dbSNP: rs537874538
rs537874538
RET
2 1.000 10 43111381 missense variant G/A snv 2.7E-04 5.6E-05 0.800 1.000 15 1994 2011
dbSNP: rs587778656
rs587778656
RET
1 1.000 10 43118436 missense variant A/C;G snv 2.0E-05; 4.0E-06 0.700 1.000 15 1994 2011
dbSNP: rs587778659
rs587778659
RET
1 1.000 10 43126720 missense variant A/G snv 1.2E-05 2.8E-05 0.700 1.000 15 1994 2011
dbSNP: rs76087194
rs76087194
RET
1 1.000 10 43120163 missense variant G/A snv 0.800 1.000 15 1994 2011
dbSNP: rs762472027
rs762472027
RET
1 1.000 10 43109046 missense variant G/A snv 8.0E-06 0.700 1.000 15 1994 2011
dbSNP: rs76534745
rs76534745
RET
1 1.000 10 43123783 missense variant A/G snv 0.800 1.000 15 1994 2011
dbSNP: rs774829203
rs774829203
RET
1 1.000 10 43106524 missense variant C/T snv 8.0E-06 2.1E-05 0.700 1.000 15 1994 2011
dbSNP: rs77596424
rs77596424
RET
1 1.000 10 43100576 missense variant C/T snv 0.800 1.000 15 1994 2011
dbSNP: rs78098482
rs78098482
RET
1 1.000 10 43109146 missense variant C/A snv 0.800 1.000 15 1994 2011
dbSNP: rs1057519052
rs1057519052
DENND3
1 1.000 8 141168410 frameshift variant G/- del 0.700 0
dbSNP: rs1057519322
rs1057519322
NCLN
1 1.000 19 3193404 stop gained C/T snv 0.700 0
dbSNP: rs1057519323
rs1057519323
NUP98
1 1.000 11 3676355 missense variant T/C snv 0.700 0
dbSNP: rs1060499894
rs1060499894
RET
1 1.000 10 43106455 missense variant G/C;T snv 0.700 0
dbSNP: rs1255575160
rs1255575160
RET
1 1.000 10 43113672 missense variant C/A snv 4.0E-06 0.700 0
dbSNP: rs1318733775
rs1318733775
RET
1 1.000 10 43119576 missense variant G/A snv 4.1E-06 7.0E-06 0.700 0
dbSNP: rs1451004715
rs1451004715
RET
1 1.000 10 43120091 missense variant G/A snv 0.700 0
dbSNP: rs1477699803
rs1477699803
RET
1 1.000 10 43100662 missense variant G/A snv 0.700 0
dbSNP: rs1553540620
rs1553540620
IHH ; MIR3131
2 1.000 2 219060317 missense variant G/T snv 0.700 0
dbSNP: rs200127630
rs200127630
RET
1 1.000 10 43119626 missense variant G/A snv 5.2E-05 2.1E-05 0.700 0
dbSNP: rs533778281
rs533778281
POLR2F
1 1.000 22 38016774 intron variant G/C snv 9.5E-04 0.700 0
dbSNP: rs541929171
rs541929171
RET
1 1.000 10 43105158 missense variant A/G snv 2.8E-05 7.0E-06 0.700 0