Variant (rsID / SNP)

rs61737841

rs61737841 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIOBP. Location: chromosome 22, position 38,167,706. Clinical significance in the table: Benign.

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Reference-table entries

TRIOBPBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 22:38167706
Cytoband: 22q13.1
HGVS: NM_001039141.3(TRIOBP):c.6899T>C (p.Val2300Ala)
Allele change: Missense_V2300A

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.