Variant (rsID / SNP)

rs61736044

rs61736044 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TENM3. Location: chromosome 4, position 183,710,332. Clinical significance in the table: Benign.

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Reference-table entries

TENM3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:183710332
Cytoband: 4q35.1
HGVS: NM_001080477.4(TENM3):c.5391G>A (p.Leu1797=)
Allele change: Synonymous_L1797L

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.