Variant (rsID / SNP)
rs2016126
rs2016126 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM104. Location: chromosome 17, position 72,784,932. The table records no clinical significance for this variant.
Reference-table entries
TMEM104Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:72784932
- HGVS
- NM_017728.4,c.172G>A,p.Val58Met
- Allele change
- Missense_V58M
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.