Variant (rsID / SNP)

rs425139

rs425139 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SEPTIN9. Location: chromosome 17, position 75,478,481. The table records no clinical significance for this variant.

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Reference-table entries

SEPTIN9Not classified

Variant type: intron_variant
Chromosome / position: 17:75478481
HGVS: NM_001113491.2,c.913+64C>T
Allele change: Silent

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.