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rs398122834

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(ACAG;ACAG) 0 common in clinvar
Make rs398122834(-;-)
Make rs398122834(-;ACAG)
ReferenceGRCh38 38.1/141
Chromosome15
Position64156108
GenePPIB, SNX22
is asnp
is mentioned by
dbSNPrs398122834
ebirs398122834
HLIrs398122834
Exacrs398122834
Varsomers398122834
Maprs398122834
PheGenIrs398122834
hapmaprs398122834
1000 genomesrs398122834
hgdprs398122834
ensemblrs398122834
gopubmedrs398122834
geneviewrs398122834
scholarrs398122834
googlers398122834
pharmgkbrs398122834
gwascentralrs398122834
openSNPrs398122834
23andMers398122834
23andMe allrs398122834
SNP Nexus

SNPshotrs398122834
SNPdbers398122834
MSV3drs398122834
GWAS Ctlgrs398122834
Max Magnitude0
ClinVar
Risk rs398122834(;)
Alt rs398122834(;)
Reference rs398122834(ACAG;ACAG)
Significance Pathogenic
Disease Osteogenesis imperfecta type 9
Variation info
Gene SNX22 PPIB
CLNDBN Osteogenesis imperfecta type 9
Reversed 1
HGVS NC_000015.9:g.64448307_64448310delCTGT
CLNSRC OMIM Allelic Variant
CLNACC RCV000034321.30,