RS75184679 RNASEH2B
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Aicardi-Goutieres syndrome 2
Aicardi Goutieres syndrome
Cerebral palsy
Abnormality of the nervous system
Autism spectrum disorder
Inborn genetic diseases
RNASEH2B-related disorder
Hereditary spastic paraplegia
Aicardi-Goutieres syndrome 2
Aicardi Goutieres syndrome
Cerebral palsy
Abnormality of the nervous system
Autism spectrum disorder
Inborn genetic diseases
RNASEH2B-related disorder
GWAS Studies (1)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| RNASEH2A protein levels | A | OR: 0.97 | 2E-45 | PubMed |
Other Variants in RNASEH2B