Variant (rsID / SNP)

rs3848596

rs3848596 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WDR88. Location: chromosome 19, position 33,635,761. The table records no clinical significance for this variant.

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Reference-table entries

WDR88Not classified

Variant type: synonymous_variant
Chromosome / position: 19:33635761
HGVS: NM_173479.4,c.399C>T,p.Asp133Asp
Allele change: Synonymous_D133D

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.