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Variant (rsID / SNP)

rs4528317

OVCH2

rs4528317 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OVCH2. Location: chromosome 11, position 7,716,855. The table records no clinical significance for this variant.

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Reference-table entries

OVCH2Not classified
Variant type
missense_variant
Chromosome / position
11:7716855
HGVS
NM_198185.7,c.1228A>T,p.Asn410Tyr
Allele change
Missense_N410Y

Public references

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