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Variant (rsID / SNP)

rs113663584

PTCH1

rs113663584 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTCH1. Location: chromosome 9, position 98,212,185. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

PTCH1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
9:98212185
Cytoband
9q22.32
HGVS
NM_000264.5(PTCH1):c.3487G>A (p.Gly1163Ser)
Allele change
Missense_G1012S

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Gorlin syndrome|Holoprosencephaly 7

Public references

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