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rs387907356

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907356(A;A)
Make rs387907356(A;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position48981411
GeneWNT1
is asnp
is mentioned by
dbSNPrs387907356
ebirs387907356
HLIrs387907356
Exacrs387907356
Varsomers387907356
Maprs387907356
PheGenIrs387907356
hapmaprs387907356
1000 genomesrs387907356
hgdprs387907356
ensemblrs387907356
gopubmedrs387907356
geneviewrs387907356
scholarrs387907356
googlers387907356
pharmgkbrs387907356
gwascentralrs387907356
openSNPrs387907356
23andMers387907356
23andMe allrs387907356
SNP Nexus

SNPshotrs387907356
SNPdbers387907356
MSV3drs387907356
GWAS Ctlgrs387907356
Max Magnitude0
ClinVar
Risk rs387907356(A;A)
Alt rs387907356(A;A)
Reference rs387907356(C;C)
Significance Pathogenic
Disease Osteogenesis imperfecta
Variation info
Gene WNT1
CLNDBN Osteogenesis imperfecta, type xv
Reversed 0
HGVS NC_000012.11:g.49375194C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000043495.30,