Have questions? Visit https://www.reddit.com/r/SNPedia

rs863225467

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TACT;TACT) 0 common in clinvar
Make rs863225467(AG;AG)
Make rs863225467(AG;TACT)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position95467134
GeneLOC100507346, PTCH1
is asnp
is mentioned by
dbSNPrs863225467
ClinGenrs863225467
ebirs863225467
HLIrs863225467
Exacrs863225467
Varsomers863225467
Maprs863225467
PheGenIrs863225467
hapmaprs863225467
1000 genomesrs863225467
hgdprs863225467
ensemblrs863225467
gopubmedrs863225467
geneviewrs863225467
scholarrs863225467
googlers863225467
pharmgkbrs863225467
gwascentralrs863225467
openSNPrs863225467
23andMers863225467
23andMe allrs863225467
SNP Nexus

SNPshotrs863225467
SNPdbers863225467
MSV3drs863225467
GWAS Ctlgrs863225467
Max Magnitude0
ClinVar
Risk rs863225467(AG;AG)
Alt rs863225467(AG;AG)
Reference Rs863225467(TACT;TACT)
Significance Pathogenic
Disease Gorlin syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene LOC100507346 PTCH1
CLNDBN Gorlin syndrome Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000009.11:g.98229416_98229419delAGTAinsCT
CLNSRC
CLNACC RCV000202420.1, RCV000492310.1,