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Variant (rsID / SNP)

rs9503893

PRPF4B

rs9503893 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRPF4B. Location: chromosome 6, position 4,031,998. The table records no clinical significance for this variant.

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Reference-table entries

PRPF4BNot classified
Variant type
missense_variant
Chromosome / position
6:4031998
HGVS
NM_003913.5,c.247A>G,p.Ile83Val
Allele change
Missense_I83V

Public references

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