Variant (rsID / SNP)

rs112888889

rs112888889 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCT. The table records no clinical significance for this variant.

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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.