Variant (rsID / SNP)
rs16940674
rs16940674 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LINC02210-CRHR1, CRHR1. Location: chromosome 17, position 43,910,507. The table records no clinical significance for this variant.
Reference-table entries
LINC02210-CRHR1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:43910507
- HGVS
- NM_001303016.1,c.471C>T,p.Cys157Cys
- Allele change
- Synonymous_C83C
Associated conditions / phenotypes
Synonymous_C83C|Synonymous_C258C|Synonymous_C218C
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.