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Variant (rsID / SNP)

rs28438857

NLRC5

rs28438857 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NLRC5. Location: chromosome 16, position 57,060,353. The table records no clinical significance for this variant.

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Reference-table entries

NLRC5Not classified
Variant type
missense_variant
Chromosome / position
16:57060353
HGVS
NM_001384950.1,c.1498T>C,p.Cys500Arg
Allele change
Missense_C500R

Public references

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