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rs121913130

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913130(A;A)
Make rs121913130(A;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position4860099
GeneMSX1
is asnp
is mentioned by
dbSNPrs121913130
ebirs121913130
HLIrs121913130
Exacrs121913130
Varsomers121913130
Maprs121913130
PheGenIrs121913130
hapmaprs121913130
1000 genomesrs121913130
hgdprs121913130
ensemblrs121913130
gopubmedrs121913130
geneviewrs121913130
scholarrs121913130
googlers121913130
pharmgkbrs121913130
gwascentralrs121913130
openSNPrs121913130
23andMers121913130
23andMe allrs121913130
SNP Nexus

SNPshotrs121913130
SNPdbers121913130
MSV3drs121913130
GWAS Ctlgrs121913130
Max Magnitude0
OMIM142983
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121913130(A;A)
Alt rs121913130(A;A)
Reference rs121913130(T;T)
Significance Pathogenic
Disease Selective tooth agenesis 1
Variation info
Gene MSX1
CLNDBN Selective tooth agenesis 1
Reversed 0
HGVS NC_000004.11:g.4861826T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000016015.21,