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rs387907325

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs387907325(-;-)
Make rs387907325(-;T)
Make rs387907325(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position41819560
GeneFKBP10
is asnp
is mentioned by
dbSNPrs387907325
ebirs387907325
HLIrs387907325
Exacrs387907325
Varsomers387907325
Maprs387907325
PheGenIrs387907325
hapmaprs387907325
1000 genomesrs387907325
hgdprs387907325
ensemblrs387907325
gopubmedrs387907325
geneviewrs387907325
scholarrs387907325
googlers387907325
pharmgkbrs387907325
gwascentralrs387907325
openSNPrs387907325
23andMers387907325
23andMe allrs387907325
SNP Nexus

SNPshotrs387907325
SNPdbers387907325
MSV3drs387907325
GWAS Ctlgrs387907325
Max Magnitude0
ClinVar
Risk rs387907325(T;T)
Alt rs387907325(T;T)
Reference rs387907325(;)
Significance Pathogenic
Disease Osteogenesis imperfecta type 11
Variation info
Gene FKBP10
CLNDBN Osteogenesis imperfecta type 11
Reversed 0
HGVS NC_000017.10:g.39975812dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000034825.6,