Variant (rsID / SNP)

rs3134587

rs3134587 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SYNM. Location: chromosome 15, position 99,670,278. The table records no clinical significance for this variant.

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Reference-table entries

SYNMNot classified

Variant type: synonymous_variant
Chromosome / position: 15:99670278
HGVS: NM_145728.3,c.1710C>T,p.Ser570Ser
Allele change: Missense_A571V

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.