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rs863223574

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223574(A;A)
Make rs863223574(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position128318879
GeneFBN2
is asnp
is mentioned by
dbSNPrs863223574
ebirs863223574
HLIrs863223574
Exacrs863223574
Varsomers863223574
Maprs863223574
PheGenIrs863223574
hapmaprs863223574
1000 genomesrs863223574
hgdprs863223574
ensemblrs863223574
gopubmedrs863223574
geneviewrs863223574
scholarrs863223574
googlers863223574
pharmgkbrs863223574
gwascentralrs863223574
openSNPrs863223574
23andMers863223574
23andMe allrs863223574
SNP Nexus

SNPshotrs863223574
SNPdbers863223574
MSV3drs863223574
GWAS Ctlgrs863223574
Max Magnitude0
ClinVar
Risk rs863223574(A;A)
Alt rs863223574(A;A)
Reference rs863223574(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN2
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.127654571C>T
CLNSRC
CLNACC RCV000197040.1,