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rs1085307511

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome9
Position95477547
GenePTCH1
is asnp
is mentioned by
dbSNPrs1085307511
dbSNP (old)rs1085307511
ClinGenrs1085307511
ebirs1085307511
HLIrs1085307511
Exacrs1085307511
Gnomadrs1085307511
Varsomers1085307511
Maprs1085307511
PheGenIrs1085307511
Biobankrs1085307511
1000 genomesrs1085307511
hgdprs1085307511
ensemblrs1085307511
gopubmedrs1085307511
geneviewrs1085307511
scholarrs1085307511
googlers1085307511
pharmgkbrs1085307511
gwascentralrs1085307511
openSNPrs1085307511
23andMers1085307511
23andMe allrs1085307511
SNPshotrs1085307511
SNPdbers1085307511
MSV3drs1085307511
GWAS Ctlgrs1085307511
Max Magnitude0
ClinVar
Risk rs1085307511(A;A)
Alt rs1085307511(A;A)
Reference Rs1085307511(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTCH1
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.98239829C>T
CLNSRC
CLNACC RCV000489836.1,