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rs121913129

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913129(C;C)
Make rs121913129(C;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position4862836
GeneMSX1
is asnp
is mentioned by
dbSNPrs121913129
ebirs121913129
HLIrs121913129
Exacrs121913129
Varsomers121913129
Maprs121913129
PheGenIrs121913129
hapmaprs121913129
1000 genomesrs121913129
hgdprs121913129
ensemblrs121913129
gopubmedrs121913129
geneviewrs121913129
scholarrs121913129
googlers121913129
pharmgkbrs121913129
gwascentralrs121913129
openSNPrs121913129
23andMers121913129
23andMe allrs121913129
SNP Nexus

SNPshotrs121913129
SNPdbers121913129
MSV3drs121913129
GWAS Ctlgrs121913129
Max Magnitude0
OMIM142983
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121913129(C;C)
Alt rs121913129(C;C)
Reference rs121913129(G;G)
Significance Pathogenic
Disease Selective tooth agenesis 1
Variation info
Gene MSX1
CLNDBN Selective tooth agenesis 1
Reversed 0
HGVS NC_000004.11:g.4864563G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000016008.25,