Variant (rsID / SNP)

rs1799724

rs1799724 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNF, LTA. Location: chromosome 6, position 31,542,482. Clinical significance in the table: risk factor.

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Reference-table entries

TNFRisk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Chromosome / position: 6:31542482
Cytoband: 6p21.33
HGVS: NM_000594.3(TNF):c.-1037C>T

Associated conditions / phenotypes

Vascular dementia, susceptibility to|Alzheimer disease, susceptibility to

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.