Variant (rsID / SNP)

rs2286394

rs2286394 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WDR55. Location: chromosome 5, position 140,048,544. The table records no clinical significance for this variant.

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Reference-table entries

WDR55Not classified

Variant type: missense_variant
Chromosome / position: 5:140048544
HGVS: NM_017706.5,c.629C>T,p.Ser210Phe
Allele change: Missense_S210F

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.