Variant (rsID / SNP)
rs26279
rs26279 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MSH3. Location: chromosome 5, position 80,168,937. Clinical significance in the table: Benign.
Reference-table entries
MSH3Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- missense_variant&splice_region_variant
- Chromosome / position
- 5:80168937
- HGVS
- NM_002439.5,c.3133G>A,p.Ala1045Thr
- Allele change
- Missense_A1045T
Associated conditions / phenotypes
Thyroid Carcinoma|Cutaneous Telangiectasia and Cancer Syndrome, Familial|Tumor Predisposition Syndrome|Inherited Cancer-Predisposing Syndrome|Myotonic Dystrophy 1|Male Infertility|Azoospermia|Hepatocellular Carcinoma|Infertility|Squamous Cell Carcinoma|Prostate Cancer|Lynch Syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.