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rs1064796259

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome9
Position95485779
GenePTCH1
is asnp
is mentioned by
dbSNPrs1064796259
dbSNP (old)rs1064796259
ClinGenrs1064796259
ebirs1064796259
HLIrs1064796259
Exacrs1064796259
Gnomadrs1064796259
Varsomers1064796259
Maprs1064796259
PheGenIrs1064796259
Biobankrs1064796259
1000 genomesrs1064796259
hgdprs1064796259
ensemblrs1064796259
gopubmedrs1064796259
geneviewrs1064796259
scholarrs1064796259
googlers1064796259
pharmgkbrs1064796259
gwascentralrs1064796259
openSNPrs1064796259
23andMers1064796259
23andMe allrs1064796259
SNPshotrs1064796259
SNPdbers1064796259
MSV3drs1064796259
GWAS Ctlgrs1064796259
Max Magnitude0
ClinVar
Risk rs1064796259(TA;TA)
Alt rs1064796259(TA;TA)
Reference Rs1064796259(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene PTCH1
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.98248061_98248062insTA
CLNSRC
CLNACC RCV000486502.1,