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Variant (rsID / SNP)

rs568922

HYOU1

rs568922 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HYOU1. Location: chromosome 11, position 118,919,206. The table records no clinical significance for this variant.

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Reference-table entries

HYOU1Not classified
Variant type
synonymous_variant
Chromosome / position
11:118919206
HGVS
NM_001130991.3,c.2235A>G,p.Ala745Ala
Allele change
Synonymous_A745A

Public references

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