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Variant (rsID / SNP)

rs372034111

UNC13D

rs372034111 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UNC13D. Location: chromosome 17, position 73,824,941. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

UNC13DConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
17:73824941
Cytoband
17q25.1
HGVS
NM_199242.3(UNC13D):c.3078C>T (p.Pro1026=)
Allele change
Synonymous_P1026P

Associated conditions / phenotypes

Familial hemophagocytic lymphohistiocytosis 3

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.