Variant (rsID / SNP)

rs949493

rs949493 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STAU2. Location: chromosome 8, position 74,527,996. The table records no clinical significance for this variant.

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Reference-table entries

STAU2Not classified

Variant type: missense_variant
Chromosome / position: 8:74527996
HGVS: NM_001164380.2,c.592G>A,p.Val198Met
Allele change: Missense_V198M

Associated conditions / phenotypes

Missense_V160M|Missense_V166M

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.