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rs137853866

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853866(A;A)
Make rs137853866(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position64160134
GenePPIB
is asnp
is mentioned by
dbSNPrs137853866
ebirs137853866
HLIrs137853866
Exacrs137853866
Varsomers137853866
Maprs137853866
PheGenIrs137853866
hapmaprs137853866
1000 genomesrs137853866
hgdprs137853866
ensemblrs137853866
gopubmedrs137853866
geneviewrs137853866
scholarrs137853866
googlers137853866
pharmgkbrs137853866
gwascentralrs137853866
openSNPrs137853866
23andMers137853866
23andMe allrs137853866
SNP Nexus

SNPshotrs137853866
SNPdbers137853866
MSV3drs137853866
GWAS Ctlgrs137853866
Max Magnitude0
ClinVar
Risk rs137853866(A;A)
Alt rs137853866(A;A)
Reference rs137853866(G;G)
Significance Pathogenic
Disease not provided Osteogenesis imperfecta type 9
Variation info
Gene PPIB
CLNDBN not provided Osteogenesis imperfecta type 9
Reversed 1
HGVS NC_000015.9:g.64452333C>T
CLNSRC OMIM Allelic Variant Osteogenesis Imperfecta Variant Database (PPIB)
CLNACC RCV000024538.1, RCV000202406.1,