Variant (rsID / SNP)
rs12637875
rs12637875 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNIK. Location: chromosome 3, position 170,893,070. The table records no clinical significance for this variant.
Reference-table entries
TNIKNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 3:170893070
- HGVS
- NM_015028.4,c.744C>T,p.Asn248Asn
- Allele change
- Synonymous_N248N
Associated conditions / phenotypes
Synonymous_N248N|Synonymous_N248N|Synonymous_N248N
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.