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rs387907355

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907355(G;T)
Make rs387907355(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position48980630
GeneWNT1
is asnp
is mentioned by
dbSNPrs387907355
ebirs387907355
HLIrs387907355
Exacrs387907355
Varsomers387907355
Maprs387907355
PheGenIrs387907355
hapmaprs387907355
1000 genomesrs387907355
hgdprs387907355
ensemblrs387907355
gopubmedrs387907355
geneviewrs387907355
scholarrs387907355
googlers387907355
pharmgkbrs387907355
gwascentralrs387907355
openSNPrs387907355
23andMers387907355
23andMe allrs387907355
SNP Nexus

SNPshotrs387907355
SNPdbers387907355
MSV3drs387907355
GWAS Ctlgrs387907355
Max Magnitude0
ClinVar
Risk rs387907355(T;T)
Alt rs387907355(T;T)
Reference rs387907355(G;G)
Significance Pathogenic
Disease Osteogenesis imperfecta
Variation info
Gene WNT1
CLNDBN Osteogenesis imperfecta, type xv
Reversed 0
HGVS NC_000012.11:g.49374413G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000043494.28,