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rs863223563

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223563(A;A)
Make rs863223563(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position128344447
GeneFBN2
is asnp
is mentioned by
dbSNPrs863223563
ebirs863223563
HLIrs863223563
Exacrs863223563
Varsomers863223563
Maprs863223563
PheGenIrs863223563
hapmaprs863223563
1000 genomesrs863223563
hgdprs863223563
ensemblrs863223563
gopubmedrs863223563
geneviewrs863223563
scholarrs863223563
googlers863223563
pharmgkbrs863223563
gwascentralrs863223563
openSNPrs863223563
23andMers863223563
23andMe allrs863223563
SNP Nexus

SNPshotrs863223563
SNPdbers863223563
MSV3drs863223563
GWAS Ctlgrs863223563
Max Magnitude0
ClinVar
Risk rs863223563(A;A)
Alt rs863223563(A;A)
Reference rs863223563(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN2
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.127680139C>T
CLNSRC
CLNACC RCV000196420.1,