Variant (rsID / SNP)

rs61823162

rs61823162 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FCRL6. Location: chromosome 1, position 159,785,413. The table records no clinical significance for this variant.

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Reference-table entries

FCRL6Not classified

Variant type: stop_gained
Chromosome / position: 1:159785413
HGVS: NM_001004310.3,c.1267C>T,p.Gln423*
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.