Variant (rsID / SNP)

rs4734653

rs4734653 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KLF10. Location: chromosome 8, position 103,663,814. The table records no clinical significance for this variant.

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Reference-table entries

KLF10Not classified

Variant type: missense_variant
Chromosome / position: 8:103663814
HGVS: NM_005655.4,c.746C>T,p.Ser249Phe
Allele change: Missense_S238F

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.