Variant (rsID / SNP)
rs6684514
rs6684514 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM79, SMG5. Location: chromosome 1, position 156,255,456. The table records no clinical significance for this variant.
Reference-table entries
TMEM79Not classified
- Variant type
- missense_variant
- Chromosome / position
- 1:156255456
- HGVS
- NM_032323.3,c.439G>A,p.Val147Met
- Allele change
- Silent
Associated conditions / phenotypes
Ige Responsiveness, Atopic|Dermatitis|Dermatitis, Atopic
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.