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rs121434559

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121434559(C;T)
Make rs121434559(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position64156802
GenePPIB, SNX22
is asnp
is mentioned by
dbSNPrs121434559
ebirs121434559
HLIrs121434559
Exacrs121434559
Varsomers121434559
Maprs121434559
PheGenIrs121434559
hapmaprs121434559
1000 genomesrs121434559
hgdprs121434559
ensemblrs121434559
gopubmedrs121434559
geneviewrs121434559
scholarrs121434559
googlers121434559
pharmgkbrs121434559
gwascentralrs121434559
openSNPrs121434559
23andMers121434559
23andMe allrs121434559
SNP Nexus

SNPshotrs121434559
SNPdbers121434559
MSV3drs121434559
GWAS Ctlgrs121434559
Max Magnitude0
OMIM123841
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121434559(T;T)
Alt rs121434559(T;T)
Reference rs121434559(C;C)
Significance Pathogenic
Disease Osteogenesis imperfecta type 9 not provided
Variation info
Gene SNX22 PPIB
CLNDBN Osteogenesis imperfecta type 9 not provided
Reversed 1
HGVS NC_000015.9:g.64449001G>A
CLNSRC OMIM Allelic Variant Osteogenesis Imperfecta Variant Database (PPIB)
CLNACC RCV000018434.25, RCV000024534.1,