RS73102625 KIF1A
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Associated Conditions
Hereditary spastic paraplegia 30
Neuropathy
hereditary sensory
type 2C
Intellectual disability
autosomal dominant 9
Inborn genetic diseases
KIF1A-related disorder
Hereditary spastic paraplegia 30
Neuropathy
hereditary sensory
type 2C
Intellectual disability
autosomal dominant 9
Inborn genetic diseases
GWAS Studies (1)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Gut microbial network clusters (Salmon (at 1 year) x Any Breastfeeding (3 Months) interaction | A | β: 0.04 | 8E-9 | PubMed |
Other Variants in KIF1A