rs397515481
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Novel de novo heterozygous FGFR1 mutation in two siblings with Hartsfield syndrome: a case of gonadal mosaicism.
|
24888332 |
2014 |
rs398122945
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Novel de novo heterozygous FGFR1 mutation in two siblings with Hartsfield syndrome: a case of gonadal mosaicism.
|
24888332 |
2014 |
rs398122946
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Novel de novo heterozygous FGFR1 mutation in two siblings with Hartsfield syndrome: a case of gonadal mosaicism.
|
24888332 |
2014 |
rs869025669
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Novel de novo heterozygous FGFR1 mutation in two siblings with Hartsfield syndrome: a case of gonadal mosaicism.
|
24888332 |
2014 |
rs869025670
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Novel de novo heterozygous FGFR1 mutation in two siblings with Hartsfield syndrome: a case of gonadal mosaicism.
|
24888332 |
2014 |
rs869025671
|
|
G |
0.800 |
CausalMutation |
CLINVAR |
Novel de novo heterozygous FGFR1 mutation in two siblings with Hartsfield syndrome: a case of gonadal mosaicism.
|
24888332 |
2014 |
rs869025671
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Novel de novo heterozygous FGFR1 mutation in two siblings with Hartsfield syndrome: a case of gonadal mosaicism.
|
24888332 |
2014 |
rs869025672
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Novel de novo heterozygous FGFR1 mutation in two siblings with Hartsfield syndrome: a case of gonadal mosaicism.
|
24888332 |
2014 |
rs397515481
|
|
G |
0.800 |
CausalMutation |
CLINVAR |
FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly.
|
23812909 |
2013 |
rs397515481
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly.
|
23812909 |
2013 |
rs398122945
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly.
|
23812909 |
2013 |
rs398122945
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly.
|
23812909 |
2013 |
rs398122946
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly.
|
23812909 |
2013 |
rs398122946
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly.
|
23812909 |
2013 |
rs869025669
|
|
G |
0.800 |
CausalMutation |
CLINVAR |
FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly.
|
23812909 |
2013 |
rs869025669
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly.
|
23812909 |
2013 |
rs869025670
|
|
G |
0.800 |
CausalMutation |
CLINVAR |
FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly.
|
23812909 |
2013 |
rs869025670
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly.
|
23812909 |
2013 |
rs869025671
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly.
|
23812909 |
2013 |
rs869025672
|
|
C |
0.800 |
CausalMutation |
CLINVAR |
FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly.
|
23812909 |
2013 |
rs869025672
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly.
|
23812909 |
2013 |
rs869025670
|
|
G |
0.800 |
GeneticVariation |
CLINVAR |
|
|
|
rs121909641
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1554548253
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1554551657
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|