Variant (rsID / SNP)

rs11790577

rs11790577 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C9ORF24, C9orf24. Location: chromosome 9, position 34,397,545. The table records no clinical significance for this variant.

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Reference-table entries

C9ORF24Not classified

Variant type: synonymous_variant
Chromosome / position: 9:34397545
HGVS: NM_032596.4,c.87T>C,p.Tyr29Tyr
Allele change: Synonymous_Y29Y

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.