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rs104893854

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893854(A;A)
Make rs104893854(A;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position4860357
GeneMSX1
is asnp
is mentioned by
dbSNPrs104893854
ebirs104893854
HLIrs104893854
Exacrs104893854
Varsomers104893854
Maprs104893854
PheGenIrs104893854
hapmaprs104893854
1000 genomesrs104893854
hgdprs104893854
ensemblrs104893854
gopubmedrs104893854
geneviewrs104893854
scholarrs104893854
googlers104893854
pharmgkbrs104893854
gwascentralrs104893854
openSNPrs104893854
23andMers104893854
23andMe allrs104893854
SNP Nexus

SNPshotrs104893854
SNPdbers104893854
MSV3drs104893854
GWAS Ctlgrs104893854
Max Magnitude0
OMIM142983
Desc
Variant0007
Relatedalso
ClinVar
Risk rs104893854(A,G;A,G)
Alt rs104893854(A,G;A,G)
Reference rs104893854(C;C)
Significance Pathogenic
Disease Orofacial cleft 5
Variation info
Gene MSX1
CLNDBN Orofacial cleft 5
Reversed 0
HGVS NC_000004.11:g.4862084C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000016014.21,