Variant (rsID / SNP)

rs365132

rs365132 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UIMC1. Location: chromosome 5, position 176,378,574. The table records no clinical significance for this variant.

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Reference-table entries

UIMC1Not classified

Variant type: synonymous_variant
Chromosome / position: 5:176378574
HGVS: NM_001199297.2,c.1344C>A,p.Thr448Thr
Allele change: Silent

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.