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rs863223606

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223606(C;C)
Make rs863223606(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position128333002
GeneFBN2
is asnp
is mentioned by
dbSNPrs863223606
ebirs863223606
HLIrs863223606
Exacrs863223606
Varsomers863223606
Maprs863223606
PheGenIrs863223606
hapmaprs863223606
1000 genomesrs863223606
hgdprs863223606
ensemblrs863223606
gopubmedrs863223606
geneviewrs863223606
scholarrs863223606
googlers863223606
pharmgkbrs863223606
gwascentralrs863223606
openSNPrs863223606
23andMers863223606
23andMe allrs863223606
SNP Nexus

SNPshotrs863223606
SNPdbers863223606
MSV3drs863223606
GWAS Ctlgrs863223606
Max Magnitude0
ClinVar
Risk rs863223606(C;C)
Alt rs863223606(C;C)
Reference rs863223606(T;T)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene FBN2
CLNDBN not specified
Reversed 1
HGVS NC_000005.9:g.127668694A>G
CLNSRC
CLNACC RCV000200404.2,