rs1031919395
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Human Fumarate Hydratase Is Dual Localized by an Alternative Transcription Initiation Mechanism.
|
27037871 |
2016 |
rs1031919395
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Fumarase: a paradigm of dual targeting and dual localized functions.
|
21929734 |
2011 |
rs1057517734
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer.
|
11865300 |
2002 |
rs1057517734
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma.
|
21398687 |
2011 |
rs1057524385
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1060499630
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1060499641
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1060499642
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1060500883
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1060500896
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1060500896
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1060500900
|
|
AG |
0.700 |
CausalMutation |
CLINVAR |
Fumarase: a paradigm of dual targeting and dual localized functions.
|
21929734 |
2011 |
rs1060500900
|
|
AG |
0.700 |
CausalMutation |
CLINVAR |
Human Fumarate Hydratase Is Dual Localized by an Alternative Transcription Initiation Mechanism.
|
27037871 |
2016 |
rs1060500900
|
|
AG |
0.700 |
CausalMutation |
CLINVAR |
Isolated cutaneous leiomyosarcoma revealing a novel germline mutation of the fumarate hydratase gene.
|
25913776 |
2016 |
rs1060500901
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma.
|
21398687 |
2011 |
rs1060500901
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Reassessing the clinical spectrum associated with hereditary leiomyomatosis and renal cell carcinoma syndrome in French FH mutation carriers.
|
28300276 |
2017 |
rs1060500901
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer.
|
11865300 |
2002 |
rs1060500901
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1060500903
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1060500904
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1060500907
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Molecular analysis and prenatal diagnosis of human fumarase deficiency.
|
9635293 |
1998 |
rs1060500907
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma.
|
21398687 |
2011 |
rs1064796708
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1131691243
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1131691246
|
|
GTTCA |
0.700 |
CausalMutation |
CLINVAR |
|
|
|