Variant (rsID / SNP)

rs3087749

rs3087749 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FOXK1. Location: chromosome 7, position 4,780,514. The table records no clinical significance for this variant.

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Reference-table entries

FOXK1Not classified

Variant type: synonymous_variant
Chromosome / position: 7:4780514
HGVS: NM_001037165.2,c.606G>T,p.Thr202Thr
Allele change: Synonymous_T202T

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.