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Variant (rsID / SNP)

rs6032259

SPINT3

rs6032259 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPINT3. Location: chromosome 20, position 44,141,331. The table records no clinical significance for this variant.

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Reference-table entries

SPINT3Not classified
Variant type
missense_variant
Chromosome / position
20:44141331
HGVS
NM_006652.2,c.230T>C,p.Leu77Ser
Allele change
Missense_L77S

Public references

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