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rs1060502286

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs1060502286(-;-)
Make rs1060502286(-;AT)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position95479006
GenePTCH1
is asnp
is mentioned by
dbSNPrs1060502286
dbSNP (old)rs1060502286
ClinGenrs1060502286
ebirs1060502286
HLIrs1060502286
Exacrs1060502286
Gnomadrs1060502286
Varsomers1060502286
Maprs1060502286
PheGenIrs1060502286
Biobankrs1060502286
1000 genomesrs1060502286
hgdprs1060502286
ensemblrs1060502286
gopubmedrs1060502286
geneviewrs1060502286
scholarrs1060502286
googlers1060502286
pharmgkbrs1060502286
gwascentralrs1060502286
openSNPrs1060502286
23andMers1060502286
23andMe allrs1060502286
SNPshotrs1060502286
SNPdbers1060502286
MSV3drs1060502286
GWAS Ctlgrs1060502286
Max Magnitude0
ClinVar
Risk rs1060502286(-;-)
Alt rs1060502286(-;-)
Reference Rs1060502286(AT;AT)
Significance Pathogenic
Disease Gorlin syndrome
Variation info
Gene PTCH1
CLNDBN Gorlin syndrome
Reversed 1
HGVS NC_000009.11:g.98241288_98241289delAT
CLNSRC
CLNACC RCV000464019.1,