Variant (rsID / SNP)

rs358231

rs358231 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GBA3. Location: chromosome 4, position 22,820,504. The table records no clinical significance for this variant.

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Reference-table entries

GBA3Not classified

Variant type: non_coding_transcript_exon_variant
Chromosome / position: 4:22820504
HGVS: NR_102355.2,n.1447A>T
Allele change: Silent

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.