Variant (rsID / SNP)

rs2273800

rs2273800 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WDR25. Location: chromosome 14, position 100,847,707. The table records no clinical significance for this variant.

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Reference-table entries

WDR25Not classified

Variant type: missense_variant
Chromosome / position: 14:100847707
HGVS: NM_001161476.3,c.446A>G,p.His149Arg
Allele change: Missense_H149R

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.