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Variant (rsID / SNP)

rs9913145

TSPOAP1

rs9913145 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSPOAP1. Location: chromosome 17, position 56,389,732. The table records no clinical significance for this variant.

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Reference-table entries

TSPOAP1Not classified
Variant type
missense_variant
Chromosome / position
17:56389732
HGVS
NM_004758.4,c.2450A>G,p.Gln817Arg
Allele change
Missense_Q757R

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.