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rs1064793698

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CC;CC) 0 common in clinvar
Chromosome9
Position95468928
GeneLOC100507346, PTCH1
is asnp
is mentioned by
dbSNPrs1064793698
dbSNP (old)rs1064793698
ClinGenrs1064793698
ebirs1064793698
HLIrs1064793698
Exacrs1064793698
Gnomadrs1064793698
Varsomers1064793698
Maprs1064793698
PheGenIrs1064793698
Biobankrs1064793698
1000 genomesrs1064793698
hgdprs1064793698
ensemblrs1064793698
gopubmedrs1064793698
geneviewrs1064793698
scholarrs1064793698
googlers1064793698
pharmgkbrs1064793698
gwascentralrs1064793698
openSNPrs1064793698
23andMers1064793698
23andMe allrs1064793698
SNPshotrs1064793698
SNPdbers1064793698
MSV3drs1064793698
GWAS Ctlgrs1064793698
Max Magnitude0
ClinVar
Risk rs1064793698(-;-)
Alt rs1064793698(-;-)
Reference Rs1064793698(CC;CC)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC100507346 PTCH1
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.98231210_98231211delGG
CLNSRC
CLNACC RCV000483987.1,