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Variant (rsID / SNP)

rs2290559

SPTBN5

rs2290559 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPTBN5. Location: chromosome 15, position 42,168,400. The table records no clinical significance for this variant.

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Reference-table entries

SPTBN5Not classified
Variant type
missense_variant
Chromosome / position
15:42168400
HGVS
NM_016642.4,c.4034G>A,p.Arg1345His
Allele change
Missense_R1345H

Public references

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