Variant (rsID / SNP)
rs2298083
rs2298083 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SMG7. Location: chromosome 1, position 183,515,428. The table records no clinical significance for this variant.
Reference-table entries
SMG7Not classified
- Variant type
- missense_variant
- Chromosome / position
- 1:183515428
- HGVS
- NM_001350220.2,c.2785G>A,p.Val929Ile
- Allele change
- Missense_V573I
Associated conditions / phenotypes
Missense_V858I|Missense_V900I|Missense_V929I|Missense_V854I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.