Variant (rsID / SNP)
rs7483
rs7483 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GSTM3. Location: chromosome 1, position 110,279,701. The table records no clinical significance for this variant.
Reference-table entries
GSTM3Not classified
- Variant type
- missense_variant
- Chromosome / position
- 1:110279701
- HGVS
- NM_000849.5,c.670G>A,p.Val224Ile
- Allele change
- Silent
Associated conditions / phenotypes
Prostate Cancer|Male Infertility|Alzheimer Disease|Mild Cognitive Impairment|Azoospermia|Renal Cell Carcinoma, Nonpapillary|Infertility
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.