Variant (rsID / SNP)

rs343376

rs343376 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FOXJ3. Location: chromosome 1, position 42,693,597. The table records no clinical significance for this variant.

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Reference-table entries

FOXJ3Not classified

Variant type: missense_variant
Chromosome / position: 1:42693597
HGVS: NM_001198850.2,c.485T>C,p.Val162Ala
Allele change: Missense_V162A

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.