Variant (rsID / SNP)
rs2740349
rs2740349 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GEMIN4. Location: chromosome 17, position 648,498. The table records no clinical significance for this variant.
Reference-table entries
GEMIN4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:648498
- HGVS
- NM_015721.3,c.2785G>A,p.Asp929Asn
- Allele change
- Missense_D929N
Associated conditions / phenotypes
Disease by Infectious Agent|Mycobacterium Tuberculosis 1|Colorectal Cancer|Lung Cancer Susceptibility 3
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.