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rs121918348

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918348(A;A)
Make rs121918348(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position129210997
GeneSMO
is asnp
is mentioned by
dbSNPrs121918348
ebirs121918348
HLIrs121918348
Exacrs121918348
Varsomers121918348
Maprs121918348
PheGenIrs121918348
hapmaprs121918348
1000 genomesrs121918348
hgdprs121918348
ensemblrs121918348
gopubmedrs121918348
geneviewrs121918348
scholarrs121918348
googlers121918348
pharmgkbrs121918348
gwascentralrs121918348
openSNPrs121918348
23andMers121918348
23andMe allrs121918348
SNP Nexus

SNPshotrs121918348
SNPdbers121918348
MSV3drs121918348
GWAS Ctlgrs121918348
Max Magnitude0
OMIM601500
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121918348(A;A)
Alt rs121918348(A;A)
Reference rs121918348(G;G)
Significance Pathogenic
Disease Basal cell carcinoma
Variation info
Gene SMO
CLNDBN Basal cell carcinoma, somatic
Reversed 0
HGVS NC_000007.13:g.128850838G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008587.4,