Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060503770
rs1060503770
SDHD
T 0.710 CausalMutation CLINVAR

dbSNP: rs5030805
rs5030805
VHL
0.710 GeneticVariation UNIPROT

dbSNP: rs5030809
rs5030809
VHL
0.710 GeneticVariation UNIPROT

dbSNP: rs79658334
rs79658334
RET
A 0.710 CausalMutation CLINVAR

dbSNP: rs104894310
rs104894310
SDHD ; TIMM8B
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060503555
rs1060503555
VHL
0.700 GeneticVariation UNIPROT

dbSNP: rs1060503752
rs1060503752
SDHB
C 0.700 CausalMutation CLINVAR

dbSNP: rs1060503753
rs1060503753
SDHB
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060503759
rs1060503759
SDHB
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060503762
rs1060503762
SDHB
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060503763
rs1060503763
SDHB
C 0.700 CausalMutation CLINVAR

dbSNP: rs1060503764
rs1060503764
SDHB
GA 0.700 CausalMutation CLINVAR

dbSNP: rs1060503769
rs1060503769
SDHD
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060503773
rs1060503773
SDHD
C 0.700 GeneticVariation CLINVAR

dbSNP: rs121908164
rs121908164
KIF1B ; LOC105376725
A 0.700 CausalMutation CLINVAR

dbSNP: rs121908813
rs121908813
CIAO1 ; TMEM127
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121908814
rs121908814
CIAO1 ; TMEM127
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121908815
rs121908815
CIAO1 ; TMEM127
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121908816
rs121908816
CIAO1 ; TMEM127
T 0.700 GeneticVariation CLINVAR

dbSNP: rs121908816
rs121908816
CIAO1 ; TMEM127
T 0.700 CausalMutation CLINVAR

dbSNP: rs121908817
rs121908817
CIAO1 ; TMEM127
CT 0.700 GeneticVariation CLINVAR

dbSNP: rs121908821
rs121908821
TMEM127
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121908822
rs121908822
TMEM127
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121908825
rs121908825
TMEM127
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121908826
rs121908826
TMEM127
G 0.700 GeneticVariation CLINVAR