Variant (rsID / SNP)

rs17360994

rs17360994 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KDF1. Location: chromosome 1, position 27,278,573. The table records no clinical significance for this variant.

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Reference-table entries

KDF1Not classified

Variant type: missense_variant
Chromosome / position: 1:27278573
HGVS: NM_152365.3,c.299A>G,p.Gln100Arg
Allele change: Missense_Q100R

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.