rs104894478
SIX1;MIR9718
BRANCHIOOTIC SYNDROME 3 (disorder)
0.800
GeneticVariation
UNIPROT
Structure-function analyses of the human SIX1-EYA2 complex reveal insights into metastasis and BOR syndrome.
23435380
2013
rs121909770
SIX1;MIR9718
BRANCHIOOTIC SYNDROME 3 (disorder)
0.800
GeneticVariation
UNIPROT
Structure-function analyses of the human SIX1-EYA2 complex reveal insights into metastasis and BOR syndrome.
23435380
2013
rs80356459
SIX1;MIR9718
BRANCHIOOTIC SYNDROME 3 (disorder)
0.800
GeneticVariation
UNIPROT
Structure-function analyses of the human SIX1-EYA2 complex reveal insights into metastasis and BOR syndrome.
23435380
2013
rs104894478
SIX1;MIR9718
BRANCHIOOTIC SYNDROME 3 (disorder)
0.800
GeneticVariation
UNIPROT
Mutation screening of the EYA1, SIX1, and SIX5 genes in a large cohort of patients harboring branchio-oto-renal syndrome calls into question the pathogenic role of SIX5 mutations.
21280147
2011
rs121909770
SIX1;MIR9718
BRANCHIOOTIC SYNDROME 3 (disorder)
0.800
GeneticVariation
UNIPROT
Mutation screening of the EYA1, SIX1, and SIX5 genes in a large cohort of patients harboring branchio-oto-renal syndrome calls into question the pathogenic role of SIX5 mutations.
21280147
2011
rs80356459
SIX1;MIR9718
BRANCHIOOTIC SYNDROME 3 (disorder)
0.800
GeneticVariation
UNIPROT
Mutation screening of the EYA1, SIX1, and SIX5 genes in a large cohort of patients harboring branchio-oto-renal syndrome calls into question the pathogenic role of SIX5 mutations.
21280147
2011
rs104894478
SIX1;MIR9718
BRANCHIOOTIC SYNDROME 3 (disorder)
0.800
GeneticVariation
UNIPROT
Biochemical and functional characterization of six SIX1 Branchio-oto-renal syndrome mutations.
19497856
2009
rs121909770
SIX1;MIR9718
BRANCHIOOTIC SYNDROME 3 (disorder)
0.800
GeneticVariation
UNIPROT
Biochemical and functional characterization of six SIX1 Branchio-oto-renal syndrome mutations.
19497856
2009
rs80356459
SIX1;MIR9718
BRANCHIOOTIC SYNDROME 3 (disorder)
0.800
GeneticVariation
UNIPROT
Biochemical and functional characterization of six SIX1 Branchio-oto-renal syndrome mutations.
19497856
2009
rs104894478
SIX1;MIR9718
BRANCHIOOTIC SYNDROME 3 (disorder)
0.800
GeneticVariation
UNIPROT
SIX1 mutation screening in 247 branchio-oto-renal syndrome families: a recurrent missense mutation associated with BOR.
18330911
2008
rs121909770
SIX1;MIR9718
BRANCHIOOTIC SYNDROME 3 (disorder)
0.800
GeneticVariation
UNIPROT
SIX1 mutation screening in 247 branchio-oto-renal syndrome families: a recurrent missense mutation associated with BOR.
18330911
2008
rs80356459
SIX1;MIR9718
BRANCHIOOTIC SYNDROME 3 (disorder)
0.800
GeneticVariation
UNIPROT
SIX1 mutation screening in 247 branchio-oto-renal syndrome families: a recurrent missense mutation associated with BOR.
18330911
2008
rs104894478
SIX1;MIR9718
BRANCHIOOTIC SYNDROME 3 (disorder)
0.800
GeneticVariation
UNIPROT
Branchio-oto-renal syndrome: detection of EYA1 and SIX1 mutations in five out of six Danish families by combining linkage, MLPA and sequencing analyses.
17637804
2007
rs121909770
SIX1;MIR9718
BRANCHIOOTIC SYNDROME 3 (disorder)
0.800
GeneticVariation
UNIPROT
Branchio-oto-renal syndrome: detection of EYA1 and SIX1 mutations in five out of six Danish families by combining linkage, MLPA and sequencing analyses.
17637804
2007
rs80356459
SIX1;MIR9718
BRANCHIOOTIC SYNDROME 3 (disorder)
0.800
GeneticVariation
UNIPROT
Branchio-oto-renal syndrome: detection of EYA1 and SIX1 mutations in five out of six Danish families by combining linkage, MLPA and sequencing analyses.
17637804
2007
rs104894478
SIX1;MIR9718
BRANCHIOOTIC SYNDROME 3 (disorder)
0.800
GeneticVariation
UNIPROT
SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes.
15141091
2004
rs121909770
SIX1;MIR9718
BRANCHIOOTIC SYNDROME 3 (disorder)
0.800
GeneticVariation
UNIPROT
SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes.
15141091
2004
rs80356459
SIX1;MIR9718
BRANCHIOOTIC SYNDROME 3 (disorder)
0.800
GeneticVariation
UNIPROT
SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes.
15141091
2004
rs104894478
SIX1;MIR9718
BRANCHIOOTIC SYNDROME 3 (disorder)
C
0.800
CausalMutation
CLINVAR
rs121909770
SIX1;MIR9718
BRANCHIOOTIC SYNDROME 3 (disorder)
T
0.800
CausalMutation
CLINVAR
rs80356459
SIX1;MIR9718
BRANCHIOOTIC SYNDROME 3 (disorder)
A
0.800
CausalMutation
CLINVAR
rs7153648
×
Entrez Id:
6495
Gene Symbol:
SIX1
SIX1
Prostate carcinoma
0.710
GeneticVariation
BEFREE
Among the 19 SNPs evaluated, 1 SNP (rs7153648 at 14q23) was associated with PCa risk [odds ratio (OR)=1.206, P<0.05)] and 1 SNP (rs636291 at 1p23) was associated with PCa aggressiveness (OR=1.123, P<0.05).
29434975
2018
rs7153648
×
Entrez Id:
6495
Gene Symbol:
SIX1
SIX1
Prostate carcinoma
C
0.710
GeneticVariation
GWASCAT
A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer.
25217961
2014
rs397515560
SIX1;MIR9718
BRANCHIOOTIC SYNDROME 3 (disorder)
0.700
GeneticVariation
UNIPROT
Structure-function analyses of the human SIX1-EYA2 complex reveal insights into metastasis and BOR syndrome.
23435380
2013
rs397515561
SIX1;MIR9718
BRANCHIOOTIC SYNDROME 3 (disorder)
0.700
GeneticVariation
UNIPROT
Structure-function analyses of the human SIX1-EYA2 complex reveal insights into metastasis and BOR syndrome.
23435380
2013