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Variant (rsID / SNP)

rs6573560

PPP1R36

rs6573560 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PPP1R36. Location: chromosome 14, position 65,031,534. The table records no clinical significance for this variant.

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Reference-table entries

PPP1R36Not classified
Variant type
missense_variant
Chromosome / position
14:65031534
HGVS
NM_172365.3,c.248C>T,p.Thr83Ile
Allele change
Missense_T83I

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.