Variant (rsID / SNP)
rs2241797
rs2241797 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TGFBRAP1. Location: chromosome 2, position 105,885,961. The table records no clinical significance for this variant.
Reference-table entries
TGFBRAP1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 2:105885961
- HGVS
- NM_001142621.3,c.2174A>G,p.His725Arg
- Allele change
- Missense_H725R
Associated conditions / phenotypes
Type 2 Diabetes Mellitus|Diabetes Mellitus
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.