Genetics University — Research, Education, Medical Genetics
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Variant (rsID / SNP)

rs45458398

GMNN

rs45458398 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GMNN. The table records no clinical significance for this variant.

Public references

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