Variant (rsID / SNP)

rs6597650

rs6597650 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FIBCD1. Location: chromosome 9, position 133,787,225. The table records no clinical significance for this variant.

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Reference-table entries

FIBCD1Not classified

Variant type: synonymous_variant
Chromosome / position: 9:133787225
HGVS: NM_001145106.2,c.900T>C,p.Asp300Asp
Allele change: Synonymous_D300D

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.