Variant (rsID / SNP)
rs7935564
rs7935564 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIM22. Location: chromosome 11, position 5,718,517. The table records no clinical significance for this variant.
Reference-table entries
TRIM22Not classified
- Variant type
- missense_variant
- Chromosome / position
- 11:5718517
- HGVS
- NM_006074.5,c.463G>A,p.Asp155Asn
- Allele change
- Missense_D155N
Associated conditions / phenotypes
Diarrhea|Hepatitis C|Hepatitis C Virus|Liver Disease|Measles|Rubella
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.