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rs869025223

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869025223(-;-)
Make rs869025223(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position41819588
GeneFKBP10
is asnp
is mentioned by
dbSNPrs869025223
ebirs869025223
HLIrs869025223
Exacrs869025223
Varsomers869025223
Maprs869025223
PheGenIrs869025223
hapmaprs869025223
1000 genomesrs869025223
hgdprs869025223
ensemblrs869025223
gopubmedrs869025223
geneviewrs869025223
scholarrs869025223
googlers869025223
pharmgkbrs869025223
gwascentralrs869025223
openSNPrs869025223
23andMers869025223
23andMe allrs869025223
SNP Nexus

SNPshotrs869025223
SNPdbers869025223
MSV3drs869025223
GWAS Ctlgrs869025223
Max Magnitude0
ClinVar
Risk rs869025223(;)
Alt rs869025223(;)
Reference rs869025223(A;A)
Significance Pathogenic
Disease Osteogenesis imperfecta
Variation info
Gene FKBP10
CLNDBN Osteogenesis imperfecta
Reversed 0
HGVS NC_000017.10:g.39975840delA
CLNSRC
CLNACC RCV000208538.1,