Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1928191
rs1928191
Entrez Id: 23500
Gene Symbol: DAAM2
DAAM2
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs2504797
rs2504797
Entrez Id: 23500
Gene Symbol: DAAM2
DAAM2
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs3004063
rs3004063
Entrez Id: 23500;100505635
Gene Symbol: DAAM2;DAAM2-AS1
DAAM2;DAAM2-AS1
CUI: C0040420
Disease:
Tonometry
A 0.700 GeneticVariation GWASCAT Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma. 29785010 2018
dbSNP: rs2504082
rs2504082
Entrez Id: 23500;100505635
Gene Symbol: DAAM2;DAAM2-AS1
DAAM2;DAAM2-AS1
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs2504800
rs2504800
Entrez Id: 23500;100505635
Gene Symbol: DAAM2;DAAM2-AS1
DAAM2;DAAM2-AS1
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs3003929
rs3003929
Entrez Id: 23500;100505635
Gene Symbol: DAAM2;DAAM2-AS1
DAAM2;DAAM2-AS1
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs3003930
rs3003930
Entrez Id: 23500;100505635
Gene Symbol: DAAM2;DAAM2-AS1
DAAM2;DAAM2-AS1
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs3003932
rs3003932
Entrez Id: 23500;100505635
Gene Symbol: DAAM2;DAAM2-AS1
DAAM2;DAAM2-AS1
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs3003938
rs3003938
Entrez Id: 23500;100505635
Gene Symbol: DAAM2;DAAM2-AS1
DAAM2;DAAM2-AS1
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs3003942
rs3003942
Entrez Id: 23500;100505635
Gene Symbol: DAAM2;DAAM2-AS1
DAAM2;DAAM2-AS1
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs2395730
rs2395730
Entrez Id: 23500
Gene Symbol: DAAM2
DAAM2
CUI: C0231921
Disease:
Pulmonary function
C 0.700 GeneticVariation GWASDB Genome-wide association study identifies five loci associated with lung function. 20010834 2010
dbSNP: rs2395730
rs2395730
Entrez Id: 23500
Gene Symbol: DAAM2
DAAM2
CUI: C0035227
Disease:
Respiratory Function Tests
C 0.700 GeneticVariation GWASCAT Genome-wide association study identifies five loci associated with lung function. 20010834 2010
dbSNP: rs2395730
rs2395730
Entrez Id: 23500
Gene Symbol: DAAM2
DAAM2
CUI: C3160731
Disease:
Pulmonary function (finding)
C 0.700 GeneticVariation GWASDB Genome-wide association study identifies five loci associated with lung function. 20010834 2010
dbSNP: rs3004070
rs3004070
Entrez Id: 4337;23500
Gene Symbol: MOCS1;DAAM2
MOCS1;DAAM2
CUI: C0856825
Disease:
Acute GVH disease
0.010 GeneticVariation BEFREE Six SNPs (rs2504787, rs2504086, rs2504082, rs3004067, rs882559, and rs3004070) of DAAM2 were associated with acute GvHD prevalence, and the genotyping was extended to larger population (N = 228). 21909696 2012
dbSNP: rs2504106
rs2504106
Entrez Id: 23500
Gene Symbol: DAAM2
DAAM2
CUI: C0279702
Disease:
Conventional (Clear Cell) Renal Cell Carcinoma
0.010 GeneticVariation BEFREE We genotyped 14 single nucleotide polymorphisms (SNPs) in 6 genes. including Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group. 19562778 2009
dbSNP: rs2504106
rs2504106
Entrez Id: 23500
Gene Symbol: DAAM2
DAAM2
CUI: C0007134
Disease:
Renal Cell Carcinoma
0.010 GeneticVariation BEFREE We genotyped 14 single nucleotide polymorphisms (SNPs) in 6 genes. including Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group. 19562778 2009
dbSNP: rs6937133
rs6937133
Entrez Id: 23500
Gene Symbol: DAAM2
DAAM2
CUI: C0007134
Disease:
Renal Cell Carcinoma
0.010 GeneticVariation BEFREE We genotyped 14 single nucleotide polymorphisms (SNPs) in 6 genes. including Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group. 19562778 2009
dbSNP: rs6937133
rs6937133
Entrez Id: 23500
Gene Symbol: DAAM2
DAAM2
CUI: C0279702
Disease:
Conventional (Clear Cell) Renal Cell Carcinoma
0.010 GeneticVariation BEFREE We genotyped 14 single nucleotide polymorphisms (SNPs) in 6 genes. including Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group. 19562778 2009