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rs1064793978

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome9
Position95477704
GenePTCH1
is asnp
is mentioned by
dbSNPrs1064793978
dbSNP (old)rs1064793978
ClinGenrs1064793978
ebirs1064793978
HLIrs1064793978
Exacrs1064793978
Gnomadrs1064793978
Varsomers1064793978
LitVarrs1064793978
Maprs1064793978
PheGenIrs1064793978
Biobankrs1064793978
1000 genomesrs1064793978
hgdprs1064793978
ensemblrs1064793978
gopubmedrs1064793978
geneviewrs1064793978
scholarrs1064793978
googlers1064793978
pharmgkbrs1064793978
gwascentralrs1064793978
openSNPrs1064793978
23andMers1064793978
23andMe allrs1064793978
SNPshotrs1064793978
SNPdbers1064793978
MSV3drs1064793978
GWAS Ctlgrs1064793978
Max Magnitude0
ClinVar
Risk rs1064793978(G;G)
Alt rs1064793978(G;G)
Reference Rs1064793978(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PTCH1
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.98239986T>C
CLNSRC
CLNACC RCV000486543.1,