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Variant (rsID / SNP)

rs61737590

TENT5B

rs61737590 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TENT5B. Location: chromosome 1, position 27,332,466. The table records no clinical significance for this variant.

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Reference-table entries

TENT5BNot classified
Variant type
missense_variant
Chromosome / position
1:27332466
HGVS
NM_052943.4,c.1247A>G,p.His416Arg
Allele change
Missense_H416R

Public references

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