rs1553602498
|
|
Dysmorphic features
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.
|
24267886 |
2013 |
rs1553521389
|
|
Dysmorphic features
|
C |
0.700 |
CausalMutation
|
CLINVAR |
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.
|
24267886 |
2013 |
rs1553602498
|
|
Dysmorphic features
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Cullin-3 regulates pattern formation, external sensory organ development and cell survival during Drosophila development.
|
15511641 |
2004 |
rs1553521389
|
|
Dysmorphic features
|
C |
0.700 |
CausalMutation
|
CLINVAR |
Cullin-3 regulates pattern formation, external sensory organ development and cell survival during Drosophila development.
|
15511641 |
2004 |
rs1553602498
|
|
Dysmorphic features
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Cullin-3 targets cyclin E for ubiquitination and controls S phase in mammalian cells.
|
10500095 |
1999 |
rs1553521389
|
|
Dysmorphic features
|
C |
0.700 |
CausalMutation
|
CLINVAR |
Cullin-3 targets cyclin E for ubiquitination and controls S phase in mammalian cells.
|
10500095 |
1999 |
rs1553602498
|
|
Dysmorphic features
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Cullin-based ubiquitin ligases: Cul3-BTB complexes join the family.
|
15071497 |
2004 |
rs1553521389
|
|
Dysmorphic features
|
C |
0.700 |
CausalMutation
|
CLINVAR |
Cullin-based ubiquitin ligases: Cul3-BTB complexes join the family.
|
15071497 |
2004 |
rs1553602498
|
|
Dysmorphic features
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Cullin3 is a KLHL10-interacting protein preferentially expressed during late spermiogenesis.
|
16162871 |
2006 |
rs1553521389
|
|
Dysmorphic features
|
C |
0.700 |
CausalMutation
|
CLINVAR |
Cullin3 is a KLHL10-interacting protein preferentially expressed during late spermiogenesis.
|
16162871 |
2006 |
rs1553602498
|
|
Dysmorphic features
|
A |
0.700 |
CausalMutation
|
CLINVAR |
De novo genic mutations among a Chinese autism spectrum disorder cohort.
|
27824329 |
2016 |
rs1553521389
|
|
Dysmorphic features
|
C |
0.700 |
CausalMutation
|
CLINVAR |
De novo genic mutations among a Chinese autism spectrum disorder cohort.
|
27824329 |
2016 |
rs1553602498
|
|
Dysmorphic features
|
A |
0.700 |
CausalMutation
|
CLINVAR |
De novo mutations in histone-modifying genes in congenital heart disease.
|
23665959 |
2013 |
rs1553521389
|
|
Dysmorphic features
|
C |
0.700 |
CausalMutation
|
CLINVAR |
De novo mutations in histone-modifying genes in congenital heart disease.
|
23665959 |
2013 |
rs1553602498
|
|
Dysmorphic features
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome).
|
24266877 |
2014 |
rs1553521389
|
|
Dysmorphic features
|
C |
0.700 |
CausalMutation
|
CLINVAR |
Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome).
|
24266877 |
2014 |
rs1553602498
|
|
Dysmorphic features
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Drosophila Kelch functions with Cullin-3 to organize the ring canal actin cytoskeleton.
|
20065088 |
2010 |
rs1553521389
|
|
Dysmorphic features
|
C |
0.700 |
CausalMutation
|
CLINVAR |
Drosophila Kelch functions with Cullin-3 to organize the ring canal actin cytoskeleton.
|
20065088 |
2010 |
rs1553602498
|
|
Dysmorphic features
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Gene expression alterations in cryptorchid males using spermatozoal microarray analysis.
|
18687424 |
2009 |
rs1553521389
|
|
Dysmorphic features
|
C |
0.700 |
CausalMutation
|
CLINVAR |
Gene expression alterations in cryptorchid males using spermatozoal microarray analysis.
|
18687424 |
2009 |
rs1553602498
|
|
Dysmorphic features
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Haploinsufficiency of kelch-like protein homolog 10 causes infertility in male mice.
|
15136734 |
2004 |
rs1553521389
|
|
Dysmorphic features
|
C |
0.700 |
CausalMutation
|
CLINVAR |
Haploinsufficiency of kelch-like protein homolog 10 causes infertility in male mice.
|
15136734 |
2004 |
rs1553602498
|
|
Dysmorphic features
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders.
|
25969726 |
2015 |
rs1553521389
|
|
Dysmorphic features
|
C |
0.700 |
CausalMutation
|
CLINVAR |
Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders.
|
25969726 |
2015 |
rs1553602498
|
|
Dysmorphic features
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Kelch proteins: emerging roles in skeletal muscle development and diseases.
|
24959344 |
2014 |