Variant (rsID / SNP)

rs55714523

rs55714523 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCYGR5. Location: chromosome 2, position 228,531,774. The table records no clinical significance for this variant.

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Reference-table entries

SCYGR5Not classified

Variant type: synonymous_variant
Chromosome / position: 2:228531774
HGVS: NM_001395406.1,c.255C>T,p.Cys85Cys

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.