Variant (rsID / SNP)

rs114583874

rs114583874 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WDR36. Location: chromosome 5, position 110,462,674. Clinical significance in the table: Likely benign.

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Reference-table entries

WDR36Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 5:110462674
Cytoband: 5q22.1
HGVS: NM_139281.3(WDR36):c.*93A>C
Allele change: Silent

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.