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Variant (rsID / SNP)

rs73011567

FCRL5

rs73011567 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FCRL5. Location: chromosome 1, position 157,504,422. The table records no clinical significance for this variant.

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Reference-table entries

FCRL5Not classified
Variant type
missense_variant
Chromosome / position
1:157504422
HGVS
NM_001195388.2,c.1663G>A,p.Val555Met
Allele change
Missense_V555M

Public references

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