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Variant (rsID / SNP)

rs228289

PIP4K2B

rs228289 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PIP4K2B. Location: chromosome 17, position 36,926,731. The table records no clinical significance for this variant.

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Reference-table entries

PIP4K2BNot classified
Variant type
synonymous_variant
Chromosome / position
17:36926731
HGVS
NM_003559.5,c.1128A>C,p.Thr376Thr
Allele change
Synonymous_T376T

Public references

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