Variant (rsID / SNP)
rs30842
rs30842 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GOT2. Location: chromosome 16, position 58,743,454. The table records no clinical significance for this variant.
Reference-table entries
GOT2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 16:58743454
- HGVS
- NM_002080.4,c.1037T>G,p.Val346Gly
- Allele change
- Missense_V346G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
