Variant (rsID / SNP)

rs3761560

rs3761560 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PAGE3. The table records no clinical significance for this variant.

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Reference-table entries

PAGE3Not classified

Variant type: synonymous_variant
HGVS: NM_001017931.3,c.255A>C,p.Gly85Gly
Allele change: Synonymous_G85G

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.