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rs387907354

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387907354(A;G)
Make rs387907354(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position48980693
GeneWNT1
is asnp
is mentioned by
dbSNPrs387907354
ebirs387907354
HLIrs387907354
Exacrs387907354
Varsomers387907354
Maprs387907354
PheGenIrs387907354
hapmaprs387907354
1000 genomesrs387907354
hgdprs387907354
ensemblrs387907354
gopubmedrs387907354
geneviewrs387907354
scholarrs387907354
googlers387907354
pharmgkbrs387907354
gwascentralrs387907354
openSNPrs387907354
23andMers387907354
23andMe allrs387907354
SNP Nexus

SNPshotrs387907354
SNPdbers387907354
MSV3drs387907354
GWAS Ctlgrs387907354
Max Magnitude0
ClinVar
Risk rs387907354(G;G)
Alt rs387907354(G;G)
Reference rs387907354(A;A)
Significance Pathogenic
Disease Osteogenesis imperfecta
Variation info
Gene WNT1
CLNDBN Osteogenesis imperfecta, type xv
Reversed 0
HGVS NC_000012.11:g.49374476A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000043493.28,