Variant (rsID / SNP)

rs3734228

rs3734228 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STX11. Location: chromosome 6, position 144,508,698. Clinical significance in the table: Benign.

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Reference-table entries

STX11Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:144508698
Cytoband: 6q24.2
HGVS: NM_003764.4(STX11):c.*70G>A
Allele change: Silent

Associated conditions / phenotypes

Familial hemophagocytic lymphohistiocytosis 4

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.