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Variant (rsID / SNP)

rs16989427

PRR14L

rs16989427 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRR14L. Location: chromosome 22, position 32,108,475. The table records no clinical significance for this variant.

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Reference-table entries

PRR14LNot classified
Variant type
missense_variant
Chromosome / position
22:32108475
HGVS
NM_173566.3,c.5350G>A,p.Val1784Ile
Allele change
Missense_V1784I

Public references

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