Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10780196
rs10780196
Entrez Id: 774
Gene Symbol: CACNA1B
CACNA1B
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: rs11137327
rs11137327
Entrez Id: 774
Gene Symbol: CACNA1B
CACNA1B
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: rs11137331
rs11137331
Entrez Id: 774
Gene Symbol: CACNA1B
CACNA1B
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: rs2168526
rs2168526
Entrez Id: 774
Gene Symbol: CACNA1B
CACNA1B
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: rs6559257
rs6559257
Entrez Id: 774
Gene Symbol: CACNA1B
CACNA1B
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: rs7023346
rs7023346
Entrez Id: 774
Gene Symbol: CACNA1B
CACNA1B
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: rs7028989
rs7028989
Entrez Id: 774
Gene Symbol: CACNA1B
CACNA1B
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs7036881
rs7036881
Entrez Id: 774
Gene Symbol: CACNA1B
CACNA1B
CUI: C0036341
Disease:
Schizophrenia
C 0.700 GeneticVariation GWASCAT Genome-wide association study of paliperidone efficacy. 27846195 2017
dbSNP: rs7040050
rs7040050
Entrez Id: 774
Gene Symbol: CACNA1B
CACNA1B
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: rs7045459
rs7045459
Entrez Id: 774
Gene Symbol: CACNA1B
CACNA1B
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: rs7046931
rs7046931
Entrez Id: 774
Gene Symbol: CACNA1B
CACNA1B
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: rs770303517
rs770303517
Entrez Id: 774
Gene Symbol: CACNA1B
CACNA1B
CUI: C1305855
Disease:
Body mass index
T 0.700 GeneticVariation GWASCAT Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. 28552196 2017
dbSNP: rs184841813
rs184841813
Entrez Id: 774
Gene Symbol: CACNA1B
CACNA1B
CUI: C1834570
Disease:
Myoclonic dystonia
0.010 GeneticVariation BEFREE These results do not support a causal association between the CACNA1B c.4166G>A; (p.R1389H) variant and M-D. 26157024 2015
dbSNP: rs10780199
rs10780199
Entrez Id: 774
Gene Symbol: CACNA1B
CACNA1B
CUI: C0007785
Disease:
Cerebral Infarction
0.010 GeneticVariation BEFREE Furthermore, the C-C-G and G-G-G haplotypes of rs7042521-rs11137351-rs10780199 were significantly more frequent in the CI group than in the control group (p = 0.024 and p < 0.000). 21166801 2010
dbSNP: rs11137351
rs11137351
Entrez Id: 774;101928786
Gene Symbol: CACNA1B;LOC101928786
CACNA1B;LOC101928786
CUI: C0007785
Disease:
Cerebral Infarction
0.010 GeneticVariation BEFREE Furthermore, the C-C-G and G-G-G haplotypes of rs7042521-rs11137351-rs10780199 were significantly more frequent in the CI group than in the control group (p = 0.024 and p < 0.000). 21166801 2010
dbSNP: rs7042521
rs7042521
Entrez Id: 774;100133077
Gene Symbol: CACNA1B;LOC100133077
CACNA1B;LOC100133077
CUI: C0007785
Disease:
Cerebral Infarction
0.010 GeneticVariation BEFREE Furthermore, the C-C-G and G-G-G haplotypes of rs7042521-rs11137351-rs10780199 were significantly more frequent in the CI group than in the control group (p = 0.024 and p < 0.000). 21166801 2010