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rs34545616

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs34545616(C;T)
Make rs34545616(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position129212026
GeneSMO
is asnp
is mentioned by
dbSNPrs34545616
ebirs34545616
HLIrs34545616
Exacrs34545616
Varsomers34545616
Maprs34545616
PheGenIrs34545616
hapmaprs34545616
1000 genomesrs34545616
hgdprs34545616
ensemblrs34545616
gopubmedrs34545616
geneviewrs34545616
scholarrs34545616
googlers34545616
pharmgkbrs34545616
gwascentralrs34545616
openSNPrs34545616
23andMers34545616
23andMe allrs34545616
SNP Nexus

SNPshotrs34545616
SNPdbers34545616
MSV3drs34545616
GWAS Ctlgrs34545616
GMAF0.003214
Max Magnitude0
Venter snp
Source plos
Gene SMO
allele T
frequency
sift
HuRef 1103652701396
Disease Association Defects in SMO are involved in basal cell carcinoma (BCC).



ClinVar
Risk rs34545616(T;T)
Alt rs34545616(T;T)
Reference rs34545616(C;C)
Significance Untested
Disease not specified
Variation info
Gene SMO
CLNDBN not specified
Reversed 0
HGVS NC_000007.13:g.128851867C>T
CLNSRC ClinVar
CLNACC RCV000122437.1,