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rs1064794117

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome9
Position95482182
GenePTCH1
is asnp
is mentioned by
dbSNPrs1064794117
dbSNP (old)rs1064794117
ClinGenrs1064794117
ebirs1064794117
HLIrs1064794117
Exacrs1064794117
Gnomadrs1064794117
Varsomers1064794117
Maprs1064794117
PheGenIrs1064794117
Biobankrs1064794117
1000 genomesrs1064794117
hgdprs1064794117
ensemblrs1064794117
gopubmedrs1064794117
geneviewrs1064794117
scholarrs1064794117
googlers1064794117
pharmgkbrs1064794117
gwascentralrs1064794117
openSNPrs1064794117
23andMers1064794117
23andMe allrs1064794117
SNPshotrs1064794117
SNPdbers1064794117
MSV3drs1064794117
GWAS Ctlgrs1064794117
Max Magnitude0
ClinVar
Risk rs1064794117(-;-)
Alt rs1064794117(-;-)
Reference Rs1064794117(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PTCH1
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.98244464delC
CLNSRC
CLNACC RCV000483470.1,