Variant (rsID / SNP)

rs140758914

rs140758914 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UNC13D. Location: chromosome 17, position 73,836,086. Clinical significance in the table: Benign.

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Reference-table entries

UNC13DBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:73836086
Cytoband: 17q25.1
HGVS: NM_199242.3(UNC13D):c.951+13T>G
Allele change: Silent

Associated conditions / phenotypes

Familial hemophagocytic lymphohistiocytosis 3

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.