Variant (rsID / SNP)

rs27141

rs27141 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PPWD1. Location: chromosome 5, position 64,881,936. The table records no clinical significance for this variant.

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Reference-table entries

PPWD1Not classified

Variant type: synonymous_variant
Chromosome / position: 5:64881936
HGVS: NM_015342.4,c.1725A>G,p.Pro575Pro
Allele change: Synonymous_P575P

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.