Variant (rsID / SNP)
rs34273689
rs34273689 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FCRL5. Location: chromosome 1, position 157,494,106. The table records no clinical significance for this variant.
Reference-table entries
FCRL5Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 1:157494106
- HGVS
- NM_001195388.2,c.2202G>A,p.Glu734Glu
- Allele change
- Synonymous_E734E
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.