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rs869320752

From SNPedia

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Geno Mag Summary
(ACT;ACT) 0 common in clinvar
Make rs869320752(-;-)
Make rs869320752(-;TAC)
Make rs869320752(TAC;TAC)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position41819359
GeneFKBP10
is asnp
is mentioned by
dbSNPrs869320752
ebirs869320752
HLIrs869320752
Exacrs869320752
Varsomers869320752
Maprs869320752
PheGenIrs869320752
hapmaprs869320752
1000 genomesrs869320752
hgdprs869320752
ensemblrs869320752
gopubmedrs869320752
geneviewrs869320752
scholarrs869320752
googlers869320752
pharmgkbrs869320752
gwascentralrs869320752
openSNPrs869320752
23andMers869320752
23andMe allrs869320752
SNP Nexus

SNPshotrs869320752
SNPdbers869320752
MSV3drs869320752
GWAS Ctlgrs869320752
Max Magnitude0
ClinVar
Risk rs869320752(;)
Alt rs869320752(;)
Reference rs869320752(ACT;ACT)
Significance Pathogenic
Disease Bruck syndrome 1
Variation info
Gene FKBP10
CLNDBN Bruck syndrome 1
Reversed 0
HGVS NC_000017.10:g.39975611_39975613delTAC
CLNSRC OMIM Allelic Variant
CLNACC RCV000190460.2,