Variant (rsID / SNP)
rs3737035
rs3737035 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NRDE2. Location: chromosome 14, position 90,745,422. The table records no clinical significance for this variant.
Reference-table entries
NRDE2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 14:90745422
- HGVS
- NM_017970.4,c.3353A>G,p.Asn1118Ser
- Allele change
- Missense_N1118S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.