Variant (rsID / SNP)

rs1133295

rs1133295 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STX8. Location: chromosome 17, position 9,471,711. The table records no clinical significance for this variant.

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Reference-table entries

STX8Not classified

Variant type: synonymous_variant
Chromosome / position: 17:9471711
HGVS: NM_004853.3,c.94A>C,p.Arg32Arg
Allele change: Synonymous_R32R

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.