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Variant (rsID / SNP)

rs9893664

STX8

rs9893664 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STX8. Location: chromosome 17, position 9,395,231. The table records no clinical significance for this variant.

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Reference-table entries

STX8Not classified
Variant type
synonymous_variant
Chromosome / position
17:9395231
HGVS
NM_004853.3,c.456C>T,p.Asp152Asp
Allele change
Synonymous_D152D

Public references

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