Variant (rsID / SNP)

rs909253

rs909253 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LTA. Location: chromosome 6, position 31,540,313. Clinical significance in the table: risk factor.

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Reference-table entries

LTARisk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Chromosome / position: 6:31540313
Cytoband: 6p21.33
HGVS: NM_000595.4(LTA):c.-10+90A>G
Allele change: Silent

Associated conditions / phenotypes

Psoriatic arthritis, susceptibility to|Myocardial infarction, 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.