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rs6446693

From SNPedia

Orientationplus
Stabilizedplus
Make rs6446693(C;C)
Make rs6446693(C;T)
Make rs6446693(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position4853353
GeneLOC100289434
is asnp
is mentioned by
dbSNPrs6446693
ebirs6446693
HLIrs6446693
Exacrs6446693
Varsomers6446693
Maprs6446693
PheGenIrs6446693
hapmaprs6446693
1000 genomesrs6446693
hgdprs6446693
ensemblrs6446693
gopubmedrs6446693
geneviewrs6446693
scholarrs6446693
googlers6446693
pharmgkbrs6446693
gwascentralrs6446693
openSNPrs6446693
23andMers6446693
23andMe allrs6446693
SNP Nexus

SNPshotrs6446693
SNPdbers6446693
MSV3drs6446693
GWAS Ctlgrs6446693
GMAF0.4394
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 20572854] MTHFR and MSX1 contribute to the risk of nonsyndromic cleft lip/palate

[PMID 20635363] Parent-of-origin effects for MSX1 in a Chilean population with nonsyndromic cleft lip/palate