Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs869025669
rs869025669
FGFR1
0.800 GeneticVariation UNIPROT FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly. 23812909

2013
dbSNP: rs869025670
rs869025670
FGFR1
G 0.800 CausalMutation CLINVAR FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly. 23812909

2013
dbSNP: rs869025670
rs869025670
FGFR1
0.800 GeneticVariation UNIPROT FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly. 23812909

2013
dbSNP: rs869025671
rs869025671
FGFR1
0.800 GeneticVariation UNIPROT FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly. 23812909

2013
dbSNP: rs869025672
rs869025672
FGFR1
C 0.800 CausalMutation CLINVAR FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly. 23812909

2013
dbSNP: rs869025672
rs869025672
FGFR1
0.800 GeneticVariation UNIPROT FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly. 23812909

2013
dbSNP: rs869025670
rs869025670
FGFR1
G 0.800 GeneticVariation CLINVAR