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

rs387907334

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387907334(G;G)
Make rs387907334(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position33120433
GeneCRTAP
is asnp
is mentioned by
dbSNPrs387907334
ebirs387907334
HLIrs387907334
Exacrs387907334
Varsomers387907334
Maprs387907334
PheGenIrs387907334
hapmaprs387907334
1000 genomesrs387907334
hgdprs387907334
ensemblrs387907334
gopubmedrs387907334
geneviewrs387907334
scholarrs387907334
googlers387907334
pharmgkbrs387907334
gwascentralrs387907334
openSNPrs387907334
23andMers387907334
23andMe allrs387907334
SNP Nexus

SNPshotrs387907334
SNPdbers387907334
MSV3drs387907334
GWAS Ctlgrs387907334
Max Magnitude0
ClinVar
Risk rs387907334(G;G)
Alt rs387907334(G;G)
Reference rs387907334(T;T)
Significance Pathogenic
Disease Osteogenesis imperfecta type 7
Variation info
Gene CRTAP
CLNDBN Osteogenesis imperfecta type 7
Reversed 0
HGVS NC_000003.11:g.33161925T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000034836.4,