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rs193922173

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922173(A;A)
Make rs193922173(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position94408220
GeneCOL1A2
is asnp
is mentioned by
dbSNPrs193922173
ebirs193922173
HLIrs193922173
Exacrs193922173
Varsomers193922173
Maprs193922173
PheGenIrs193922173
hapmaprs193922173
1000 genomesrs193922173
hgdprs193922173
ensemblrs193922173
gopubmedrs193922173
geneviewrs193922173
scholarrs193922173
googlers193922173
pharmgkbrs193922173
gwascentralrs193922173
openSNPrs193922173
23andMers193922173
23andMe allrs193922173
SNP Nexus

SNPshotrs193922173
SNPdbers193922173
MSV3drs193922173
GWAS Ctlgrs193922173
Max Magnitude0
ClinVar
Risk rs193922173(A;A)
Alt rs193922173(A;A)
Reference rs193922173(G;G)
Significance Probable-Pathogenic
Disease Osteogenesis imperfecta
Variation info
Gene COL1A2
CLNDBN Osteogenesis imperfecta
Reversed 0
HGVS NC_000007.13:g.94037532G>A
CLNSRC ClinVar LabCorp
CLNACC RCV000029611.1,