Variant (rsID / SNP)
rs4950394
rs4950394 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CHD1L. Location: chromosome 1, position 146,767,149. The table records no clinical significance for this variant.
Reference-table entries
CHD1LNot classified
- Variant type
- missense_variant
- Chromosome / position
- 1:146767149
- HGVS
- NM_004284.6,c.2653G>T,p.Ala885Ser
- Allele change
- Silent
Associated conditions / phenotypes
Missense_A604S|Silent|Missense_A604S|Missense_A785S|Silent|Missense_A772S|Silent|Missense_A604S|Missense_A604S|Missense_A604S|Silent|Missense_A772S|Missense_A681S|Silent|Missense_A604S|Silent|Missense_A722S|Missense_A604S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.