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rs1064793922

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome9
Position95482198
GenePTCH1
is asnp
is mentioned by
dbSNPrs1064793922
dbSNP (old)rs1064793922
ClinGenrs1064793922
ebirs1064793922
HLIrs1064793922
Exacrs1064793922
Gnomadrs1064793922
Varsomers1064793922
LitVarrs1064793922
Maprs1064793922
PheGenIrs1064793922
Biobankrs1064793922
1000 genomesrs1064793922
hgdprs1064793922
ensemblrs1064793922
gopubmedrs1064793922
geneviewrs1064793922
scholarrs1064793922
googlers1064793922
pharmgkbrs1064793922
gwascentralrs1064793922
openSNPrs1064793922
23andMers1064793922
23andMe allrs1064793922
SNPshotrs1064793922
SNPdbers1064793922
MSV3drs1064793922
GWAS Ctlgrs1064793922
Max Magnitude0
ClinVar
Risk rs1064793922(A;A)
Alt rs1064793922(A;A)
Reference Rs1064793922(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PTCH1
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.98244480C>T
CLNSRC
CLNACC RCV000478704.1,