Variant (rsID / SNP)
rs3740918
rs3740918 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIRREL3. Location: chromosome 11, position 126,310,156. The table records no clinical significance for this variant.
Reference-table entries
KIRREL3Not classified
- Variant type
- intron_variant
- Chromosome / position
- 11:126310156
- HGVS
- NM_032531.4,c.1353+188C>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.