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rs387907357

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs387907357(-;-)
Make rs387907357(-;AACA)
Make rs387907357(AACA;AACA)
ReferenceGRCh38 38.1/141
Chromosome12
Position48981476
GeneWNT1
is asnp
is mentioned by
dbSNPrs387907357
ebirs387907357
HLIrs387907357
Exacrs387907357
Varsomers387907357
Maprs387907357
PheGenIrs387907357
hapmaprs387907357
1000 genomesrs387907357
hgdprs387907357
ensemblrs387907357
gopubmedrs387907357
geneviewrs387907357
scholarrs387907357
googlers387907357
pharmgkbrs387907357
gwascentralrs387907357
openSNPrs387907357
23andMers387907357
23andMe allrs387907357
SNP Nexus

SNPshotrs387907357
SNPdbers387907357
MSV3drs387907357
GWAS Ctlgrs387907357
Max Magnitude0
ClinVar
Risk rs387907357(AACA;AACA)
Alt rs387907357(AACA;AACA)
Reference rs387907357(;)
Significance Pathogenic
Disease Osteogenesis imperfecta
Variation info
Gene WNT1
CLNDBN Osteogenesis imperfecta, type xv
Reversed 0
HGVS NC_000012.11:g.49375256_49375259dupAACA
CLNSRC OMIM Allelic Variant
CLNACC RCV000043496.29,