Variant (rsID / SNP)

rs34331240

rs34331240 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WDR25. Location: chromosome 14, position 100,847,617. The table records no clinical significance for this variant.

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Reference-table entries

WDR25Not classified

Variant type: missense_variant
Chromosome / position: 14:100847617
HGVS: NM_001161476.3,c.356C>T,p.Thr119Met
Allele change: Missense_T119M

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.