Variant (rsID / SNP)

rs34312177

rs34312177 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GBA2, RGP1. Location: chromosome 9, position 35,748,669. Clinical significance in the table: Benign.

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Reference-table entries

GBA2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 9:35748669
Cytoband: 9p13.3
HGVS: NM_020944.3(GBA2):c.33C>T (p.Thr11=)
Allele change: Synonymous_T11T

Associated conditions / phenotypes

Spastic paraplegia

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.