Variant (rsID / SNP)

rs28580141

rs28580141 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to INPP5B. Location: chromosome 1, position 38,353,941. The table records no clinical significance for this variant.

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Reference-table entries

INPP5BNot classified

Variant type: synonymous_variant
Chromosome / position: 1:38353941
HGVS: NM_001365820.1,c.873C>A,p.Ile291Ile
Allele change: Synonymous_I71I

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.