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rs397509383

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CC;CC) 0 common in clinvar
Make rs397509383(A;A)
Make rs397509383(A;CC)
ReferenceGRCh38 38.1/141
Chromosome17
Position41820961
GeneFKBP10
is asnp
is mentioned by
dbSNPrs397509383
ebirs397509383
HLIrs397509383
Exacrs397509383
Varsomers397509383
Maprs397509383
PheGenIrs397509383
hapmaprs397509383
1000 genomesrs397509383
hgdprs397509383
ensemblrs397509383
gopubmedrs397509383
geneviewrs397509383
scholarrs397509383
googlers397509383
pharmgkbrs397509383
gwascentralrs397509383
openSNPrs397509383
23andMers397509383
23andMe allrs397509383
SNP Nexus

SNPshotrs397509383
SNPdbers397509383
MSV3drs397509383
GWAS Ctlgrs397509383
Max Magnitude0
ClinVar
Risk rs397509383(A;A)
Alt rs397509383(A;A)
Reference rs397509383(CC;CC)
Significance Pathogenic
Disease Bruck syndrome 1 Osteogenesis imperfecta type 11
Variation info
Gene FKBP10
CLNDBN Bruck syndrome 1 Osteogenesis imperfecta type 11
Reversed 0
HGVS NC_000017.10:g.39977213_39977214delCCinsA
CLNSRC OMIM Allelic Variant
CLNACC RCV000034324.5, RCV000034359.4,