Variant (rsID / SNP)

rs12975322

rs12975322 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBN3. Location: chromosome 19, position 8,176,640. The table records no clinical significance for this variant.

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Reference-table entries

FBN3Not classified

Variant type: missense_variant
Chromosome / position: 19:8176640
HGVS: NM_001321431.2,c.3976G>A,p.Val1326Ile
Allele change: Missense_V1326I

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.