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Variant (rsID / SNP)

rs1456235

SPTBN5

rs1456235 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPTBN5. Location: chromosome 15, position 42,149,472. The table records no clinical significance for this variant.

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Reference-table entries

SPTBN5Not classified
Variant type
missense_variant
Chromosome / position
15:42149472
HGVS
NM_016642.4,c.8585A>G,p.Gln2862Arg
Allele change
Missense_Q2862R

Public references

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