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rs193922159

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922159(A;A)
Make rs193922159(A;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position94410478
GeneCOL1A2
is asnp
is mentioned by
dbSNPrs193922159
ebirs193922159
HLIrs193922159
Exacrs193922159
Varsomers193922159
Maprs193922159
PheGenIrs193922159
hapmaprs193922159
1000 genomesrs193922159
hgdprs193922159
ensemblrs193922159
gopubmedrs193922159
geneviewrs193922159
scholarrs193922159
googlers193922159
pharmgkbrs193922159
gwascentralrs193922159
openSNPrs193922159
23andMers193922159
23andMe allrs193922159
SNP Nexus

SNPshotrs193922159
SNPdbers193922159
MSV3drs193922159
GWAS Ctlgrs193922159
Max Magnitude0
ClinVar
Risk rs193922159(A;A)
Alt rs193922159(A;A)
Reference rs193922159(C;C)
Significance Probable-Pathogenic
Disease Osteogenesis imperfecta
Variation info
Gene COL1A2
CLNDBN Osteogenesis imperfecta
Reversed 0
HGVS NC_000007.13:g.94039790C>A
CLNSRC ClinVar LabCorp
CLNACC RCV000029589.1,