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rs863223603

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223603(G;G)
Make rs863223603(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position128338075
GeneFBN2
is asnp
is mentioned by
dbSNPrs863223603
ebirs863223603
HLIrs863223603
Exacrs863223603
Varsomers863223603
Maprs863223603
PheGenIrs863223603
hapmaprs863223603
1000 genomesrs863223603
hgdprs863223603
ensemblrs863223603
gopubmedrs863223603
geneviewrs863223603
scholarrs863223603
googlers863223603
pharmgkbrs863223603
gwascentralrs863223603
openSNPrs863223603
23andMers863223603
23andMe allrs863223603
SNP Nexus

SNPshotrs863223603
SNPdbers863223603
MSV3drs863223603
GWAS Ctlgrs863223603
Max Magnitude0
ClinVar
Risk rs863223603(G;G)
Alt rs863223603(G;G)
Reference rs863223603(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN2
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.127673767A>C
CLNSRC
CLNACC RCV000197957.1,