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rs863223568

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223568(C;C)
Make rs863223568(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position128336056
GeneFBN2
is asnp
is mentioned by
dbSNPrs863223568
ebirs863223568
HLIrs863223568
Exacrs863223568
Varsomers863223568
Maprs863223568
PheGenIrs863223568
hapmaprs863223568
1000 genomesrs863223568
hgdprs863223568
ensemblrs863223568
gopubmedrs863223568
geneviewrs863223568
scholarrs863223568
googlers863223568
pharmgkbrs863223568
gwascentralrs863223568
openSNPrs863223568
23andMers863223568
23andMe allrs863223568
SNP Nexus

SNPshotrs863223568
SNPdbers863223568
MSV3drs863223568
GWAS Ctlgrs863223568
Max Magnitude0
ClinVar
Risk rs863223568(C;C)
Alt rs863223568(C;C)
Reference rs863223568(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN2
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.127671748A>G
CLNSRC
CLNACC RCV000198913.1,