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rs121918347

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918347(G;T)
Make rs121918347(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position129210500
GeneSMO
is asnp
is mentioned by
dbSNPrs121918347
ebirs121918347
HLIrs121918347
Exacrs121918347
Varsomers121918347
Maprs121918347
PheGenIrs121918347
hapmaprs121918347
1000 genomesrs121918347
hgdprs121918347
ensemblrs121918347
gopubmedrs121918347
geneviewrs121918347
scholarrs121918347
googlers121918347
pharmgkbrs121918347
gwascentralrs121918347
openSNPrs121918347
23andMers121918347
23andMe allrs121918347
SNP Nexus

SNPshotrs121918347
SNPdbers121918347
MSV3drs121918347
GWAS Ctlgrs121918347
Max Magnitude0
OMIM601500
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918347(T;T)
Alt rs121918347(T;T)
Reference rs121918347(G;G)
Significance Pathogenic
Disease Basal cell carcinoma
Variation info
Gene SMO
CLNDBN Basal cell carcinoma, somatic
Reversed 0
HGVS NC_000007.13:g.128850341G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008586.5,