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

rs75059851

IGSF9B

rs75059851 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IGSF9B. 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.