Variant (rsID / SNP)

rs2273801

rs2273801 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WDR25. Location: chromosome 14, position 100,847,437. The table records no clinical significance for this variant.

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Reference-table entries

WDR25Not classified

Variant type: missense_variant
Chromosome / position: 14:100847437
HGVS: NM_001161476.3,c.176A>G,p.Lys59Arg
Allele change: Missense_K59R

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.