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rs863223572

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223572(C;T)
Make rs863223572(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position128330669
GeneFBN2
is asnp
is mentioned by
dbSNPrs863223572
ebirs863223572
HLIrs863223572
Exacrs863223572
Varsomers863223572
Maprs863223572
PheGenIrs863223572
hapmaprs863223572
1000 genomesrs863223572
hgdprs863223572
ensemblrs863223572
gopubmedrs863223572
geneviewrs863223572
scholarrs863223572
googlers863223572
pharmgkbrs863223572
gwascentralrs863223572
openSNPrs863223572
23andMers863223572
23andMe allrs863223572
SNP Nexus

SNPshotrs863223572
SNPdbers863223572
MSV3drs863223572
GWAS Ctlgrs863223572
Max Magnitude0
ClinVar
Risk rs863223572(T;T)
Alt rs863223572(T;T)
Reference rs863223572(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN2
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.127666361G>A
CLNSRC
CLNACC RCV000198694.1,