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rs368869806

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs368869806(C;T)
Make rs368869806(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position95485875
GenePTCH1
is asnp
is mentioned by
dbSNPrs368869806
ebirs368869806
HLIrs368869806
Exacrs368869806
Varsomers368869806
Maprs368869806
PheGenIrs368869806
hapmaprs368869806
1000 genomesrs368869806
hgdprs368869806
ensemblrs368869806
gopubmedrs368869806
geneviewrs368869806
scholarrs368869806
googlers368869806
pharmgkbrs368869806
gwascentralrs368869806
openSNPrs368869806
23andMers368869806
23andMe allrs368869806
SNP Nexus

SNPshotrs368869806
SNPdbers368869806
MSV3drs368869806
GWAS Ctlgrs368869806
Max Magnitude0
ClinVar
Risk rs368869806(T;T)
Alt rs368869806(T;T)
Reference rs368869806(C;C)
Significance Probable-Pathogenic
Disease Gorlin syndrome
Variation info
Gene PTCH1
CLNDBN Gorlin syndrome
Reversed 0
HGVS NC_000009.11:g.98248157C>T
CLNSRC
CLNACC RCV000149897.1,