Variant (rsID / SNP)

rs33204

rs33204 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WDR41. Location: chromosome 5, position 76,734,084. The table records no clinical significance for this variant.

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Reference-table entries

WDR41Not classified

Variant type: missense_variant
Chromosome / position: 5:76734084
HGVS: NM_018268.4,c.985G>A,p.Val329Ile
Allele change: Missense_V329I

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.