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rs1085307752

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome9
Position95479148
GenePTCH1
is asnp
is mentioned by
dbSNPrs1085307752
dbSNP (old)rs1085307752
ClinGenrs1085307752
ebirs1085307752
HLIrs1085307752
Exacrs1085307752
Gnomadrs1085307752
Varsomers1085307752
LitVarrs1085307752
Maprs1085307752
PheGenIrs1085307752
Biobankrs1085307752
1000 genomesrs1085307752
hgdprs1085307752
ensemblrs1085307752
gopubmedrs1085307752
geneviewrs1085307752
scholarrs1085307752
googlers1085307752
pharmgkbrs1085307752
gwascentralrs1085307752
openSNPrs1085307752
23andMers1085307752
23andMe allrs1085307752
SNPshotrs1085307752
SNPdbers1085307752
MSV3drs1085307752
GWAS Ctlgrs1085307752
Max Magnitude0
ClinVar
Risk rs1085307752(A;A)
Alt rs1085307752(A;A)
Reference Rs1085307752(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene PTCH1
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000009.11:g.98241430C>A; NC_000009.11:g.98241430C>T
CLNSRC
CLNACC RCV000492636.1, RCV000489555.1,