Variant (rsID / SNP)

rs3750010

rs3750010 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PAPOLB, RADIL. Location: chromosome 7, position 4,901,191. The table records no clinical significance for this variant.

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Reference-table entries

PAPOLBNot classified

Variant type: missense_variant
Chromosome / position: 7:4901191
HGVS: NM_020144.5,c.251A>G,p.Lys84Arg
Allele change: Silent

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.