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rs1064796618

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome9
Position95461858
GeneLOC100507346, PTCH1
is asnp
is mentioned by
dbSNPrs1064796618
dbSNP (old)rs1064796618
ClinGenrs1064796618
ebirs1064796618
HLIrs1064796618
Exacrs1064796618
Gnomadrs1064796618
Varsomers1064796618
Maprs1064796618
PheGenIrs1064796618
Biobankrs1064796618
1000 genomesrs1064796618
hgdprs1064796618
ensemblrs1064796618
gopubmedrs1064796618
geneviewrs1064796618
scholarrs1064796618
googlers1064796618
pharmgkbrs1064796618
gwascentralrs1064796618
openSNPrs1064796618
23andMers1064796618
23andMe allrs1064796618
SNPshotrs1064796618
SNPdbers1064796618
MSV3drs1064796618
GWAS Ctlgrs1064796618
Max Magnitude0
ClinVar
Risk rs1064796618(T;T)
Alt rs1064796618(T;T)
Reference Rs1064796618(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC100507346 PTCH1
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.98224140G>A
CLNSRC
CLNACC RCV000480196.1,