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rs878853856

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878853856(C;C)
Make rs878853856(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position95453533
GenePTCH1
is asnp
is mentioned by
dbSNPrs878853856
ebirs878853856
HLIrs878853856
Exacrs878853856
Varsomers878853856
Maprs878853856
PheGenIrs878853856
hapmaprs878853856
1000 genomesrs878853856
hgdprs878853856
ensemblrs878853856
gopubmedrs878853856
geneviewrs878853856
scholarrs878853856
googlers878853856
pharmgkbrs878853856
gwascentralrs878853856
openSNPrs878853856
23andMers878853856
23andMe allrs878853856
SNP Nexus

SNPshotrs878853856
SNPdbers878853856
MSV3drs878853856
GWAS Ctlgrs878853856
Max Magnitude0
ClinVar
Risk rs878853856(C;C)
Alt rs878853856(C;C)
Reference rs878853856(T;T)
Significance Probable-Pathogenic
Disease Gorlin syndrome
Variation info
Gene PTCH1
CLNDBN Gorlin syndrome
Reversed 1
HGVS NC_000009.11:g.98215815A>G
CLNSRC
CLNACC RCV000226160.1,