Variant (rsID / SNP)
rs2296160
rs2296160 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CR1. Location: chromosome 1, position 207,795,320. The table records no clinical significance for this variant.
Reference-table entries
CR1Not classified
- Variant type
- missense_variant&splice_region_variant
- Chromosome / position
- 1:207795320
- HGVS
- NM_000651.6,c.7255A>G,p.Thr2419Ala
- Allele change
- Missense_T1969A
Associated conditions / phenotypes
Malaria|Interstitial Lung Disease 2|Alzheimer Disease|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.