Variant (rsID / SNP)

rs377095569

rs377095569 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FLNB. Location: chromosome 3, position 58,116,643. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

FLNBBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 3:58116643
Cytoband: 3p14.3
HGVS: NM_001457.4(FLNB):c.4390+8T>A
Allele change: Silent

Associated conditions / phenotypes

FLNB-Related Spectrum Disorders

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.