Variant (rsID / SNP)

rs3733548

rs3733548 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SEPSECS. Location: chromosome 4, position 25,156,483. Clinical significance in the table: Benign.

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Reference-table entries

SEPSECSBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:25156483
Cytoband: 4p15.2
HGVS: NM_016955.4(SEPSECS):c.701+137T>C
Allele change: Silent

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.