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rs104894052

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894052(C;C)
Make rs104894052(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position155803294
GeneSHH
is asnp
is mentioned by
dbSNPrs104894052
ebirs104894052
HLIrs104894052
Exacrs104894052
Varsomers104894052
Maprs104894052
PheGenIrs104894052
hapmaprs104894052
1000 genomesrs104894052
hgdprs104894052
ensemblrs104894052
gopubmedrs104894052
geneviewrs104894052
scholarrs104894052
googlers104894052
pharmgkbrs104894052
gwascentralrs104894052
openSNPrs104894052
23andMers104894052
23andMe allrs104894052
SNP Nexus

SNPshotrs104894052
SNPdbers104894052
MSV3drs104894052
GWAS Ctlgrs104894052
Max Magnitude0
OMIM600725
Desc
Variant0018
Relatedalso
ClinVar
Risk rs104894052(C;C)
Alt rs104894052(C;C)
Reference rs104894052(T;T)
Significance Pathogenic
Disease Single upper central incisor
Variation info
Gene SHH
CLNDBN Single upper central incisor
Reversed 1
HGVS NC_000007.13:g.155595988A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000009444.2,