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rs104893852

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893852(A;A)
Make rs104893852(A;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position4860231
GeneMSX1
is asnp
is mentioned by
dbSNPrs104893852
ebirs104893852
HLIrs104893852
Exacrs104893852
Varsomers104893852
Maprs104893852
PheGenIrs104893852
hapmaprs104893852
1000 genomesrs104893852
hgdprs104893852
ensemblrs104893852
gopubmedrs104893852
geneviewrs104893852
scholarrs104893852
googlers104893852
pharmgkbrs104893852
gwascentralrs104893852
openSNPrs104893852
23andMers104893852
23andMe allrs104893852
SNP Nexus

SNPshotrs104893852
SNPdbers104893852
MSV3drs104893852
GWAS Ctlgrs104893852
Max Magnitude0
OMIM142983
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104893852(A;A)
Alt rs104893852(A;A)
Reference rs104893852(C;C)
Significance Pathogenic
Disease Tooth agenesis
Variation info
Gene MSX1
CLNDBN Tooth agenesis, selective, with or without orofacial cleft
Reversed 0
HGVS NC_000004.11:g.4861958C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000016009.25,