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Variant (rsID / SNP)

rs8104955

SIGLEC5

rs8104955 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SIGLEC5. Location: chromosome 19, position 52,130,788. The table records no clinical significance for this variant.

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Reference-table entries

SIGLEC5Not classified
Variant type
synonymous_variant
Chromosome / position
19:52130788
HGVS
NM_003830.4,c.1209C>T,p.Ser403Ser
Allele change
Synonymous_S403S

Public references

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