Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs75996173
rs75996173
RET
A 0.850 CausalMutation CLINVAR

dbSNP: rs75996173
rs75996173
RET
T 0.850 CausalMutation CLINVAR

dbSNP: rs75996173
rs75996173
RET
C 0.850 CausalMutation CLINVAR

dbSNP: rs77724903
rs77724903
RET
0.830 GeneticVariation UNIPROT

dbSNP: rs77724903
rs77724903
RET
T 0.830 CausalMutation CLINVAR

dbSNP: rs75076352
rs75076352
RET
C 0.820 CausalMutation CLINVAR

dbSNP: rs75076352
rs75076352
RET
G 0.820 CausalMutation CLINVAR

dbSNP: rs5030824
rs5030824
VHL
0.810 GeneticVariation UNIPROT

dbSNP: rs5030824
rs5030824
VHL
G 0.810 CausalMutation CLINVAR

dbSNP: rs104893826
rs104893826
VHL
0.800 GeneticVariation UNIPROT

dbSNP: rs104893826
rs104893826
VHL
C 0.800 CausalMutation CLINVAR

dbSNP: rs121908827
rs121908827
TMEM127
G 0.800 GeneticVariation CLINVAR

dbSNP: rs121908828
rs121908828
TMEM127
T 0.800 GeneticVariation CLINVAR

dbSNP: rs121917755
rs121917755
SDHB
A 0.800 CausalMutation CLINVAR

dbSNP: rs397516440
rs397516440
VHL
G 0.800 GeneticVariation CLINVAR

dbSNP: rs5030808
rs5030808
VHL
A 0.800 CausalMutation CLINVAR

dbSNP: rs5030820
rs5030820
VHL
0.800 GeneticVariation UNIPROT

dbSNP: rs5030820
rs5030820
VHL
T 0.800 CausalMutation CLINVAR

dbSNP: rs74315371
rs74315371
SDHB
T 0.800 CausalMutation CLINVAR

dbSNP: rs772551056
rs772551056
SDHB
0.800 GeneticVariation UNIPROT

dbSNP: rs77709286
rs77709286
RET
G 0.800 CausalMutation CLINVAR

dbSNP: rs77709286
rs77709286
RET
0.800 GeneticVariation UNIPROT

dbSNP: rs786202732
rs786202732
SDHB
G 0.800 CausalMutation CLINVAR

dbSNP: rs74799832
rs74799832
RET
C 0.740 CausalMutation CLINVAR

dbSNP: rs76262710
rs76262710
RET
G 0.720 CausalMutation CLINVAR