Variant (rsID / SNP)

rs168939

rs168939 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZFYVE16. Location: chromosome 5, position 79,735,858. The table records no clinical significance for this variant.

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Reference-table entries

ZFYVE16Not classified

Variant type: missense_variant
Chromosome / position: 5:79735858
HGVS: NM_001284237.2,c.2426A>G,p.Tyr809Cys
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.