Variant (rsID / SNP)
rs910925
rs910925 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GEMIN4. Location: chromosome 17, position 649,547. The table records no clinical significance for this variant.
Reference-table entries
GEMIN4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:649547
- HGVS
- NM_015721.3,c.1736C>G,p.Ala579Gly
- Allele change
- Missense_A579G
Associated conditions / phenotypes
Renal Cell Carcinoma, Nonpapillary
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.