Variant (rsID / SNP)
rs7954976
rs7954976 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BIN2. Location: chromosome 12, position 51,681,903. The table records no clinical significance for this variant.
Reference-table entries
BIN2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 12:51681903
- HGVS
- NM_016293.4,c.1585A>G,p.Asn529Asp
- Allele change
- Missense_N475D
Associated conditions / phenotypes
Missense_N529D|Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.