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Variant (rsID / SNP)

rs6482626

PTCHD3

rs6482626 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTCHD3. Location: chromosome 10, position 27,702,725. The table records no clinical significance for this variant.

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Reference-table entries

PTCHD3Not classified
Variant type
missense_variant
Chromosome / position
10:27702725
HGVS
NM_001034842.5,c.455T>C,p.Leu152Pro
Allele change
Missense_L152P

Public references

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