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Variant (rsID / SNP)

rs9890721

MYCBPAP

rs9890721 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYCBPAP. Location: chromosome 17, position 48,603,503. The table records no clinical significance for this variant.

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Reference-table entries

MYCBPAPNot classified
Variant type
missense_variant
Chromosome / position
17:48603503
HGVS
NM_001366294.2,c.2089C>T,p.Arg697Trp
Allele change
Missense_R725W

Public references

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