Variant (rsID / SNP)

rs525420

rs525420 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRR36. Location: chromosome 19, position 7,936,208. The table records no clinical significance for this variant.

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Reference-table entries

PRR36Not classified

Variant type: missense_variant
Chromosome / position: 19:7936208
HGVS: NM_001190467.2,c.1919T>C,p.Ile640Thr
Allele change: Missense_S641P

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.