Variant (rsID / SNP)

rs202081420

rs202081420 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTCH1. Location: chromosome 9, position 98,221,872. 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: 9:98221872
Cytoband: 9q22.32
HGVS: NM_000264.5(PTCH1):c.2887+10G>A
Allele change: Silent

Associated conditions / phenotypes

Gorlin syndrome|Holoprosencephaly 7

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.