Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12239874
rs12239874
Entrez Id: 374977;100527960
Gene Symbol: MROH7;MROH7-TTC4
MROH7;MROH7-TTC4
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs17110938
rs17110938
Entrez Id: 374977;100527960
Gene Symbol: MROH7;MROH7-TTC4
MROH7;MROH7-TTC4
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs646356
rs646356
Entrez Id: 374977;100527960
Gene Symbol: MROH7;MROH7-TTC4
MROH7;MROH7-TTC4
CUI: C0004096
Disease:
Asthma
0.700 GeneticVariation GWASCAT Identification of Four Novel Loci in Asthma in European American and African American Populations. 27611488 2017
dbSNP: rs6671173
rs6671173
Entrez Id: 374977;100527960
Gene Symbol: MROH7;MROH7-TTC4
MROH7;MROH7-TTC4
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs6671173
rs6671173
Entrez Id: 374977;100527960
Gene Symbol: MROH7;MROH7-TTC4
MROH7;MROH7-TTC4
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs744746
rs744746
Entrez Id: 374977;100527960
Gene Symbol: MROH7;MROH7-TTC4
MROH7;MROH7-TTC4
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs744748
rs744748
Entrez Id: 374977;100527960
Gene Symbol: MROH7;MROH7-TTC4
MROH7;MROH7-TTC4
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs879063
rs879063
Entrez Id: 374977;100527960
Gene Symbol: MROH7;MROH7-TTC4
MROH7;MROH7-TTC4
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs61768793
rs61768793
Entrez Id: 7268;100527960
Gene Symbol: TTC4;MROH7-TTC4
TTC4;MROH7-TTC4
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012