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rs137853869

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AAGA;AAGA) 0 common in clinvar
Make rs137853869(-;-)
Make rs137853869(-;AAGA)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position64156115
GenePPIB, SNX22
is asnp
is mentioned by
dbSNPrs137853869
dbSNP (old)rs137853869
ClinGenrs137853869
ebirs137853869
HLIrs137853869
Exacrs137853869
Gnomadrs137853869
Varsomers137853869
Maprs137853869
PheGenIrs137853869
Biobankrs137853869
1000 genomesrs137853869
hgdprs137853869
ensemblrs137853869
gopubmedrs137853869
geneviewrs137853869
scholarrs137853869
googlers137853869
pharmgkbrs137853869
gwascentralrs137853869
openSNPrs137853869
23andMers137853869
23andMe allrs137853869
SNP Nexus

SNPshotrs137853869
SNPdbers137853869
MSV3drs137853869
GWAS Ctlgrs137853869
Max Magnitude0
ClinVar
Risk rs137853869(-;-)
Alt rs137853869(-;-)
Reference Rs137853869(AAGA;AAGA)
Significance Pathogenic
Disease Osteogenesis imperfecta type 9 not provided
Variation info
Gene PPIB SNX22
CLNDBN Osteogenesis imperfecta type 9 not provided
Reversed 1
HGVS NC_000015.9:g.64448314_64448317delTCTT
CLNSRC OMIM Allelic Variant
CLNACC RCV000018433.27, RCV000024535.1,