Variant (rsID / SNP)

rs2972191

rs2972191 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FOXD1. Location: chromosome 5, position 72,742,882. The table records no clinical significance for this variant.

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Reference-table entries

FOXD1Not classified

Variant type: synonymous_variant
Chromosome / position: 5:72742882
HGVS: NM_004472.3,c.1305A>G,p.Ser435Ser
Allele change: Missense_S436G

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.