Variant (rsID / SNP)

rs12984133

rs12984133 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRR36. Location: chromosome 19, position 7,935,716. The table records no clinical significance for this variant.

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Reference-table entries

PRR36Not classified

Variant type: missense_variant
Chromosome / position: 19:7935716
HGVS: NM_001190467.2,c.2411C>T,p.Thr804Met
Allele change: Missense_R805C

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.