Variant (rsID / SNP)
rs684260
rs684260 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C1ORF109, C1orf109. Location: chromosome 1, position 38,148,765. The table records no clinical significance for this variant.
Reference-table entries
C1ORF109Not classified
- Variant type
- missense_variant
- Chromosome / position
- 1:38148765
- HGVS
- NM_001350755.2,c.835T>C,p.Tyr279His
- Allele change
- Missense_Y279H
Associated conditions / phenotypes
Missense_Y216H|Silent|Missense_Y278H|Silent|Silent|Missense_Y216H|Missense_Y216H|Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.