Variant (rsID / SNP)
rs7547279
rs7547279 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CHD1L. Location: chromosome 1, position 146,751,782. The table records no clinical significance for this variant.
Reference-table entries
CHD1LNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 1:146751782
- HGVS
- NM_004284.6,c.1623A>C,p.Ile541Ile
- Allele change
- Silent
Associated conditions / phenotypes
Synonymous_I260I|Silent|Synonymous_I260I|Synonymous_I441I|Silent|Synonymous_I428I|Silent|Synonymous_I260I|Synonymous_I260I|Synonymous_I260I|Silent|Synonymous_I428I|Synonymous_I337I|Silent|Synonymous_I260I|Silent|Synonymous_I378I|Synonymous_I260I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.