Variant (rsID / SNP)

rs41274480

rs41274480 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PGD. Location: chromosome 1, position 10,479,791. The table records no clinical significance for this variant.

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Reference-table entries

PGDNot classified

Variant type: synonymous_variant
Chromosome / position: 1:10479791
HGVS: NM_002631.4,c.1437G>A,p.Ser479Ser
Allele change: Synonymous_S457S

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.