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rs1064795637

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GAGT;GAGT) 0 common in clinvar
Chromosome9
Position95480384
GenePTCH1
is asnp
is mentioned by
dbSNPrs1064795637
dbSNP (old)rs1064795637
ClinGenrs1064795637
ebirs1064795637
HLIrs1064795637
Exacrs1064795637
Gnomadrs1064795637
Varsomers1064795637
LitVarrs1064795637
Maprs1064795637
PheGenIrs1064795637
Biobankrs1064795637
1000 genomesrs1064795637
hgdprs1064795637
ensemblrs1064795637
gopubmedrs1064795637
geneviewrs1064795637
scholarrs1064795637
googlers1064795637
pharmgkbrs1064795637
gwascentralrs1064795637
openSNPrs1064795637
23andMers1064795637
23andMe allrs1064795637
SNPshotrs1064795637
SNPdbers1064795637
MSV3drs1064795637
GWAS Ctlgrs1064795637
Max Magnitude0
ClinVar
Risk rs1064795637(-;-)
Alt rs1064795637(-;-)
Reference Rs1064795637(GAGT;GAGT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTCH1
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.98242666_98242669delACTC
CLNSRC
CLNACC RCV000479558.1,