Variant (rsID / SNP)
rs2149171
rs2149171 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NTNG2. Location: chromosome 9, position 135,102,254. The table records no clinical significance for this variant.
Reference-table entries
NTNG2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 9:135102254
- HGVS
- NM_032536.4,c.876C>T,p.His292His
- Allele change
- Synonymous_H292H
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.