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rs137853864

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137853864(G;G)
Make rs137853864(G;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position64162961
GenePPIB
is asnp
is mentioned by
dbSNPrs137853864
ebirs137853864
HLIrs137853864
Exacrs137853864
Varsomers137853864
Maprs137853864
PheGenIrs137853864
hapmaprs137853864
1000 genomesrs137853864
hgdprs137853864
ensemblrs137853864
gopubmedrs137853864
geneviewrs137853864
scholarrs137853864
googlers137853864
pharmgkbrs137853864
gwascentralrs137853864
openSNPrs137853864
23andMers137853864
23andMe allrs137853864
SNP Nexus

SNPshotrs137853864
SNPdbers137853864
MSV3drs137853864
GWAS Ctlgrs137853864
Max Magnitude0
ClinVar
Risk rs137853864(G;G)
Alt rs137853864(G;G)
Reference rs137853864(T;T)
Significance Pathogenic
Disease Osteogenesis imperfecta type 9 not provided
Variation info
Gene PPIB
CLNDBN Osteogenesis imperfecta type 9 not provided
Reversed 1
HGVS NC_000015.9:g.64455160A>C
CLNSRC OMIM Allelic Variant Osteogenesis Imperfecta Variant Database (PPIB)
CLNACC RCV000018435.28, RCV000024544.1,