Variant (rsID / SNP)

rs1056847

rs1056847 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PI4KB. Location: chromosome 1, position 151,288,172. The table records no clinical significance for this variant.

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Reference-table entries

PI4KBNot classified

Variant type: synonymous_variant
Chromosome / position: 1:151288172
HGVS: NM_001369626.1,c.786C>T,p.Asp262Asp
Allele change: Synonymous_D262D

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.