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rs372896892

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs372896892(C;T)
Make rs372896892(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position41820412
GeneFKBP10
is asnp
is mentioned by
dbSNPrs372896892
ebirs372896892
HLIrs372896892
Exacrs372896892
Varsomers372896892
Maprs372896892
PheGenIrs372896892
hapmaprs372896892
1000 genomesrs372896892
hgdprs372896892
ensemblrs372896892
gopubmedrs372896892
geneviewrs372896892
scholarrs372896892
googlers372896892
pharmgkbrs372896892
gwascentralrs372896892
openSNPrs372896892
23andMers372896892
23andMe allrs372896892
SNP Nexus

SNPshotrs372896892
SNPdbers372896892
MSV3drs372896892
GWAS Ctlgrs372896892
Max Magnitude0
ClinVar
Risk rs372896892(G,T;G,T)
Alt rs372896892(G,T;G,T)
Reference rs372896892(C;C)
Significance Pathogenic
Disease Osteogenesis imperfecta type 11
Variation info
Gene FKBP10
CLNDBN Osteogenesis imperfecta type 11
Reversed 0
HGVS NC_000017.10:g.39976664C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000033069.3,