Variant (rsID / SNP)
rs11870849
rs11870849 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ENDOV. Location: chromosome 17, position 78,411,073. The table records no clinical significance for this variant.
Reference-table entries
ENDOVNot classified
- Variant type
- 3_prime_UTR_variant
- Chromosome / position
- 17:78411073
- HGVS
- NM_001164637.3,c.*1130C>T
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.