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rs121912766

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912766(C;T)
Make rs121912766(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position53950222
GeneBMP4
is asnp
is mentioned by
dbSNPrs121912766
ebirs121912766
HLIrs121912766
Exacrs121912766
Varsomers121912766
Maprs121912766
PheGenIrs121912766
hapmaprs121912766
1000 genomesrs121912766
hgdprs121912766
ensemblrs121912766
gopubmedrs121912766
geneviewrs121912766
scholarrs121912766
googlers121912766
pharmgkbrs121912766
gwascentralrs121912766
openSNPrs121912766
23andMers121912766
23andMe allrs121912766
SNP Nexus

SNPshotrs121912766
SNPdbers121912766
MSV3drs121912766
GWAS Ctlgrs121912766
Max Magnitude0
OMIM112262
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121912766(T;T)
Alt rs121912766(T;T)
Reference rs121912766(C;C)
Significance Pathogenic
Disease Orofacial cleft 11
Variation info
Gene BMP4 MIR5580
CLNDBN Orofacial cleft 11
Reversed 1
HGVS NC_000014.8:g.54416940G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019276.27,