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

rs137853943

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853943(A;A)
Make rs137853943(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position33114550
GeneCRTAP
is asnp
is mentioned by
dbSNPrs137853943
ebirs137853943
HLIrs137853943
Exacrs137853943
Varsomers137853943
Maprs137853943
PheGenIrs137853943
hapmaprs137853943
1000 genomesrs137853943
hgdprs137853943
ensemblrs137853943
gopubmedrs137853943
geneviewrs137853943
scholarrs137853943
googlers137853943
pharmgkbrs137853943
gwascentralrs137853943
openSNPrs137853943
23andMers137853943
23andMe allrs137853943
SNP Nexus

SNPshotrs137853943
SNPdbers137853943
MSV3drs137853943
GWAS Ctlgrs137853943
Max Magnitude0
ClinVar
Risk rs137853943(A;A)
Alt rs137853943(A;A)
Reference rs137853943(C;C)
Significance Pathogenic
Disease Osteogenesis imperfecta type 7
Variation info
Gene CRTAP
CLNDBN Osteogenesis imperfecta type 7
Reversed 0
HGVS NC_000003.11:g.33156042C>A; NC_000003.11:g.33156042C>G
CLNSRC
CLNACC RCV000190575.1, RCV000192794.1,