Variant (rsID / SNP)

rs7245429

rs7245429 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBN3. Location: chromosome 19, position 8,159,362. The table records no clinical significance for this variant.

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Reference-table entries

FBN3Not classified

Variant type: missense_variant
Chromosome / position: 19:8159362
HGVS: NM_001321431.2,c.5873C>A,p.Pro1958His
Allele change: Missense_P1958H

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.