Variant (rsID / SNP)

rs1131356

rs1131356 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FLNB. Location: chromosome 3, position 58,109,162. Clinical significance in the table: Benign.

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Reference-table entries

FLNBBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:58109162
Cytoband: 3p14.3
HGVS: NM_001457.4(FLNB):c.3469G>A (p.Asp1157Asn)
Allele change: Missense_D1157N

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.