Variant (rsID / SNP)

rs13360277

rs13360277 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UIMC1. Location: chromosome 5, position 176,370,402. The table records no clinical significance for this variant.

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Reference-table entries

UIMC1Not classified

Variant type: missense_variant
Chromosome / position: 5:176370402
HGVS: NM_001199297.2,c.1531T>C,p.Cys511Arg
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.