Variant (rsID / SNP)

rs13176855

rs13176855 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NIM1K. Location: chromosome 5, position 43,245,922. The table records no clinical significance for this variant.

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Reference-table entries

NIM1KNot classified

Variant type: synonymous_variant
Chromosome / position: 5:43245922
HGVS: NM_153361.4,c.45C>T,p.His15His
Allele change: Synonymous_H15H

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.