Variant (rsID / SNP)

rs2185379

rs2185379 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRDM1. Location: chromosome 6, position 106,536,253. The table records no clinical significance for this variant.

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Reference-table entries

PRDM1Not classified

Variant type: single nucleotide variant
Chromosome / position: 6:106536253
Cytoband: 6q21
HGVS: NM_001198.4(PRDM1):c.220G>A (p.Gly74Ser)
Allele change: Missense_G74S

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.