Variant (rsID / SNP)

rs17275986

rs17275986 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SEMA3C. Location: chromosome 7, position 80,418,689. The table records no clinical significance for this variant.

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Reference-table entries

SEMA3CNot classified

Variant type: synonymous_variant
Chromosome / position: 7:80418689
HGVS: NM_001350120.2,c.1341T>C,p.Tyr447Tyr
Allele change: Synonymous_Y371Y

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.