Variant (rsID / SNP)
rs17036325
rs17036325 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CALM2. Location: chromosome 2, position 47,390,058. Clinical significance in the table: Benign.
Reference-table entries
CALM2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:47390058
- Cytoband
- 2p21
- HGVS
- NM_001743.6(CALM2):c.35-257A>G
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.