Variant (rsID / SNP)
rs1778541
rs1778541 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VN1R5. Location: chromosome 1, position 247,419,664. The table records no clinical significance for this variant.
Reference-table entries
VN1R5Not classified
- Variant type
- non_coding_transcript_exon_variant
- Chromosome / position
- 1:247419664
- HGVS
- NR_160309.1,n.291C>T
- Allele change
- Synonymous_T97T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.