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

rs121912768

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912768(A;A)
Make rs121912768(A;G)
ReferenceGRCh38 38.1/142
Chromosome14
Position53950399
GeneBMP4
is asnp
is mentioned by
dbSNPrs121912768
ebirs121912768
HLIrs121912768
Exacrs121912768
Varsomers121912768
Maprs121912768
PheGenIrs121912768
hapmaprs121912768
1000 genomesrs121912768
hgdprs121912768
ensemblrs121912768
gopubmedrs121912768
geneviewrs121912768
scholarrs121912768
googlers121912768
pharmgkbrs121912768
gwascentralrs121912768
openSNPrs121912768
23andMers121912768
23andMe allrs121912768
SNP Nexus

SNPshotrs121912768
SNPdbers121912768
MSV3drs121912768
GWAS Ctlgrs121912768
GMAF0.0009183
Max Magnitude0
OMIM112262
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121912768(A;A)
Alt rs121912768(A;A)
Reference rs121912768(G;G)
Significance Pathogenic
Disease Orofacial cleft 11
Variation info
Gene BMP4 MIR5580
CLNDBN Orofacial cleft 11
Reversed 1
HGVS NC_000014.8:g.54417117C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019278.24,