Variant (rsID / SNP)

rs150445941

rs150445941 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FLNB. Location: chromosome 3, position 58,118,639. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

FLNBConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 3:58118639
Cytoband: 3p14.3
HGVS: NM_001457.4(FLNB):c.4495G>A (p.Asp1499Asn)
Allele change: Missense_D1499N

Associated conditions / phenotypes

FLNB-Related Spectrum Disorders|Connective tissue disorder

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.