Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387907105
rs387907105
Entrez Id: 9841
Gene Symbol: ZBTB24
ZBTB24
CUI: C3279748
Disease:
IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 2 		0.800 GeneticVariation UNIPROT Mutations in ZBTB24 are associated with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2. 21596365 2011
dbSNP: rs387907105
rs387907105
Entrez Id: 9841
Gene Symbol: ZBTB24
ZBTB24
CUI: C3279748
Disease:
IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 2 		C 0.800 CausalMutation CLINVAR
dbSNP: rs12203098
rs12203098
Entrez Id: 9841
Gene Symbol: ZBTB24
ZBTB24
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs12203098
rs12203098
Entrez Id: 9841
Gene Symbol: ZBTB24
ZBTB24
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1046943
rs1046943
Entrez Id: 9841;64780
Gene Symbol: ZBTB24;MICAL1
ZBTB24;MICAL1
CUI: C0005890
Disease:
Body Height 		A 0.700 GeneticVariation GWASCAT Hundreds of variants clustered in genomic loci and biological pathways affect human height. 20881960 2010
dbSNP: rs1046943
rs1046943
Entrez Id: 9841;64780
Gene Symbol: ZBTB24;MICAL1
ZBTB24;MICAL1
CUI: C0489786
Disease:
Height 		A 0.700 GeneticVariation GWASDB Hundreds of variants clustered in genomic loci and biological pathways affect human height. 20881960 2010
dbSNP: rs370370334
rs370370334
Entrez Id: 9841;105377935
Gene Symbol: ZBTB24;LOC105377935
ZBTB24;LOC105377935
CUI: C3279748
Disease:
IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 2 		C 0.700 CausalMutation CLINVAR
dbSNP: rs387907104
rs387907104
Entrez Id: 9841
Gene Symbol: ZBTB24
ZBTB24
CUI: C3279748
Disease:
IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 2 		A 0.700 CausalMutation CLINVAR
dbSNP: rs387907106
rs387907106
Entrez Id: 9841;64780
Gene Symbol: ZBTB24;MICAL1
ZBTB24;MICAL1
CUI: C3279748
Disease:
IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 2 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1046943
rs1046943
Entrez Id: 9841;64780
Gene Symbol: ZBTB24;MICAL1
ZBTB24;MICAL1
CUI: C0853193
Disease:
Bipolar I disorder 		0.010 GeneticVariation BEFREE The strongest findings occurred at 6q21 (non-parametric pairs LOD 3.4 for rs1046943 at 119 cM) and 9q21 (non-parametric pairs logarithm of odds (LOD) 3.4 for rs722642 at 78 cM) using only BPI and schizoaffective (SA), BP cases. 21769101 2012