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rs104894049

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104894049(A;T)
Make rs104894049(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position155806527
GeneSHH
is asnp
is mentioned by
dbSNPrs104894049
ebirs104894049
HLIrs104894049
Exacrs104894049
Varsomers104894049
Maprs104894049
PheGenIrs104894049
hapmaprs104894049
1000 genomesrs104894049
hgdprs104894049
ensemblrs104894049
gopubmedrs104894049
geneviewrs104894049
scholarrs104894049
googlers104894049
pharmgkbrs104894049
gwascentralrs104894049
openSNPrs104894049
23andMers104894049
23andMe allrs104894049
SNP Nexus

SNPshotrs104894049
SNPdbers104894049
MSV3drs104894049
GWAS Ctlgrs104894049
Max Magnitude0
OMIM600725
Desc
Variant0014
Relatedalso
ClinVar
Risk rs104894049(T;T)
Alt rs104894049(T;T)
Reference rs104894049(A;A)
Significance Pathogenic
Disease Single upper central incisor
Variation info
Gene SHH
CLNDBN Single upper central incisor
Reversed 1
HGVS NC_000007.13:g.155599221T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009440.2,



[PMID 26590974] Relation between sonic hedgehog pathway gene polymorphisms and basal cell carcinoma development in the Polish population