Variant (rsID / SNP)

rs61741210

rs61741210 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSPOAP1. Location: chromosome 17, position 56,386,732. Clinical significance in the table: Benign.

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Reference-table entries

TSPOAP1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:56386732
Cytoband: 17q22
HGVS: NM_004758.4(TSPOAP1):c.3901G>A (p.Asp1301Asn)
Allele change: Missense_D1241N

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.