Variant (rsID / SNP)

rs260087

rs260087 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SYNM. Location: chromosome 15, position 99,671,760. The table records no clinical significance for this variant.

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Reference-table entries

SYNMNot classified

Variant type: synonymous_variant
Chromosome / position: 15:99671760
HGVS: NM_145728.3,c.3192T>C,p.Phe1064Phe
Allele change: Missense_L1065S

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.