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Variant (rsID / SNP)

rs4984639

TPSG1

rs4984639 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TPSG1. Location: chromosome 16, position 1,272,865. The table records no clinical significance for this variant.

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Reference-table entries

TPSG1Not classified
Variant type
synonymous_variant
Chromosome / position
16:1272865
HGVS
NM_012467.4,c.298C>T,p.Leu100Leu
Allele change
Synonymous_L100L

Public references

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