Variant (rsID / SNP)
rs2075820
rs2075820 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NOD1. Location: chromosome 7, position 30,492,237. The table records no clinical significance for this variant.
Reference-table entries
NOD1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 7:30492237
- HGVS
- NM_006092.4,c.796G>A,p.Glu266Lys
- Allele change
- Silent
Associated conditions / phenotypes
Gastric Cancer|Helicobacter Pylori Infection|Childhood-Onset Asthma|Asthma|Malaria|Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets|Peptic Ulcer Disease|Crohn's Disease|Bladder Cancer|Multiple Sclerosis|Gastritis|Relapsing-Remitting Multiple Sclerosis|Skin Carcinoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.