Variant (rsID / SNP)
rs1036199
rs1036199 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HAVCR2. Location: chromosome 5, position 156,531,736. The table records no clinical significance for this variant.
Reference-table entries
HAVCR2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 5:156531736
- HGVS
- NM_032782.5,c.419G>T,p.Arg140Leu
- Allele change
- Missense_R140L
Associated conditions / phenotypes
Autoimmune Disease|Rheumatoid Arthritis|Crohn's Disease|Arthritis|Squamous Cell Carcinoma|Ovarian Cancer|Ovarian Epithelial Cancer
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.