Variant (rsID / SNP)
rs7186832
rs7186832 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIM72. Location: chromosome 16, position 31,230,463. The table records no clinical significance for this variant.
Reference-table entries
TRIM72Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 16:31230463
- HGVS
- NM_001008274.4,c.438C>T,p.Arg146Arg
- Allele change
- Synonymous_R146R
Associated conditions / phenotypes
Type 2 Diabetes Mellitus
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.