Variant (rsID / SNP)
rs7971718
rs7971718 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OVOS2. Location: chromosome 12, position 31,310,983. The table records no clinical significance for this variant.
Reference-table entries
OVOS2Not classified
- Variant type
- non_coding_transcript_exon_variant
- Chromosome / position
- 12:31310983
- HGVS
- NR_153414.1,n.2054C>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.