Variant (rsID / SNP)

rs1760897

rs1760897 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TEP1. Location: chromosome 14, position 20,876,253. The table records no clinical significance for this variant.

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Reference-table entries

TEP1Not classified

Variant type: missense_variant
Chromosome / position: 14:20876253
HGVS: NM_007110.5,c.346T>C,p.Ser116Pro
Allele change: Missense_S116P

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.