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rs1064794260

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome9
Position95459654
GenePTCH1
is asnp
is mentioned by
dbSNPrs1064794260
dbSNP (old)rs1064794260
ClinGenrs1064794260
ebirs1064794260
HLIrs1064794260
Exacrs1064794260
Gnomadrs1064794260
Varsomers1064794260
Maprs1064794260
PheGenIrs1064794260
Biobankrs1064794260
1000 genomesrs1064794260
hgdprs1064794260
ensemblrs1064794260
gopubmedrs1064794260
geneviewrs1064794260
scholarrs1064794260
googlers1064794260
pharmgkbrs1064794260
gwascentralrs1064794260
openSNPrs1064794260
23andMers1064794260
23andMe allrs1064794260
SNPshotrs1064794260
SNPdbers1064794260
MSV3drs1064794260
GWAS Ctlgrs1064794260
Max Magnitude0
ClinVar
Risk rs1064794260(T;T)
Alt rs1064794260(T;T)
Reference Rs1064794260(C;C)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene PTCH1
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000009.11:g.98221936G>A
CLNSRC
CLNACC RCV000479378.1, RCV000492276.1,