Variant (rsID / SNP)
rs3737002
rs3737002 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CR1. Location: chromosome 1, position 207,760,773. The table records no clinical significance for this variant.
Reference-table entries
CR1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 1:207760773
- HGVS
- NM_000651.6,c.5573C>T,p.Thr1858Met
- Allele change
- Missense_T1408M
Associated conditions / phenotypes
Alzheimer Disease|Interstitial Lung Disease 2|Mild Cognitive Impairment|Leprosy 3|Fibrosis of Extraocular Muscles, Congenital, 1|Hepatocellular Carcinoma|Pulmonary Fibrosis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.