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rs863223565

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223565(A;A)
Make rs863223565(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position128338949
GeneFBN2
is asnp
is mentioned by
dbSNPrs863223565
ebirs863223565
HLIrs863223565
Exacrs863223565
Varsomers863223565
Maprs863223565
PheGenIrs863223565
hapmaprs863223565
1000 genomesrs863223565
hgdprs863223565
ensemblrs863223565
gopubmedrs863223565
geneviewrs863223565
scholarrs863223565
googlers863223565
pharmgkbrs863223565
gwascentralrs863223565
openSNPrs863223565
23andMers863223565
23andMe allrs863223565
SNP Nexus

SNPshotrs863223565
SNPdbers863223565
MSV3drs863223565
GWAS Ctlgrs863223565
Max Magnitude0
ClinVar
Risk rs863223565(A;A)
Alt rs863223565(A;A)
Reference rs863223565(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN2
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.127674641C>T
CLNSRC
CLNACC RCV000200568.1,