Variant (rsID / SNP)

rs17686437

rs17686437 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OTOR. Location: chromosome 20, position 16,729,048. Clinical significance in the table: Benign.

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Reference-table entries

OTORBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 20:16729048
Cytoband: 20p12.1
HGVS: NM_020157.4(OTOR):c.2T>C (p.Met1Thr)
Allele change: Missense_M1T

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.