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rs863223566

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223566(A;C)
Make rs863223566(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position128338029
GeneFBN2
is asnp
is mentioned by
dbSNPrs863223566
ebirs863223566
HLIrs863223566
Exacrs863223566
Varsomers863223566
Maprs863223566
PheGenIrs863223566
hapmaprs863223566
1000 genomesrs863223566
hgdprs863223566
ensemblrs863223566
gopubmedrs863223566
geneviewrs863223566
scholarrs863223566
googlers863223566
pharmgkbrs863223566
gwascentralrs863223566
openSNPrs863223566
23andMers863223566
23andMe allrs863223566
SNP Nexus

SNPshotrs863223566
SNPdbers863223566
MSV3drs863223566
GWAS Ctlgrs863223566
Max Magnitude0
ClinVar
Risk rs863223566(C;C)
Alt rs863223566(C;C)
Reference rs863223566(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN2
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.127673721T>G
CLNSRC
CLNACC RCV000198884.1,