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Variant (rsID / SNP)

rs754382

VPS37C

rs754382 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VPS37C. Location: chromosome 11, position 60,899,767. The table records no clinical significance for this variant.

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Reference-table entries

VPS37CNot classified
Variant type
missense_variant
Chromosome / position
11:60899767
HGVS
NM_017966.5,c.593T>C,p.Leu198Ser
Allele change
Missense_L198S

Public references

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