Have questions? Visit https://www.reddit.com/r/SNPedia

rs104893850

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893850(C;T)
Make rs104893850(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position4862808
GeneMSX1
is asnp
is mentioned by
dbSNPrs104893850
ebirs104893850
HLIrs104893850
Exacrs104893850
Varsomers104893850
Maprs104893850
PheGenIrs104893850
hapmaprs104893850
1000 genomesrs104893850
hgdprs104893850
ensemblrs104893850
gopubmedrs104893850
geneviewrs104893850
scholarrs104893850
googlers104893850
pharmgkbrs104893850
gwascentralrs104893850
openSNPrs104893850
23andMers104893850
23andMe allrs104893850
SNP Nexus

SNPshotrs104893850
SNPdbers104893850
MSV3drs104893850
GWAS Ctlgrs104893850
Max Magnitude0
OMIM142983
Desc
Variant0006
Relatedalso
ClinVar
Risk rs104893850(T;T)
Alt rs104893850(T;T)
Reference rs104893850(C;C)
Significance Pathogenic
Disease Selective tooth agenesis 1
Variation info
Gene MSX1
CLNDBN Selective tooth agenesis 1
Reversed 0
HGVS NC_000004.11:g.4864535C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000016010.25,