Variant (rsID / SNP)

rs201945549

rs201945549 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRDM5. Location: chromosome 4, position 121,774,625. Clinical significance in the table: Uncertain significance.

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Reference-table entries

PRDM5Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 4:121774625
Cytoband: 4q27
HGVS: NM_018699.4(PRDM5):c.248G>A (p.Arg83His)
Allele change: Missense_R83H

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.