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Variant (rsID / SNP)

rs149667902

PTCH1

rs149667902 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTCH1. Location: chromosome 9, position 98,209,298. 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
9:98209298
Cytoband
9q22.32
HGVS
NM_000264.5(PTCH1):c.4240G>A (p.Val1414Met)
Allele change
Missense_V1263M

Associated conditions / phenotypes

Gorlin syndrome|Hereditary cancer-predisposing syndrome|Holoprosencephaly 7

Public references

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