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rs863223605

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223605(G;T)
Make rs863223605(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position128334719
GeneFBN2
is asnp
is mentioned by
dbSNPrs863223605
ebirs863223605
HLIrs863223605
Exacrs863223605
Varsomers863223605
Maprs863223605
PheGenIrs863223605
hapmaprs863223605
1000 genomesrs863223605
hgdprs863223605
ensemblrs863223605
gopubmedrs863223605
geneviewrs863223605
scholarrs863223605
googlers863223605
pharmgkbrs863223605
gwascentralrs863223605
openSNPrs863223605
23andMers863223605
23andMe allrs863223605
SNP Nexus

SNPshotrs863223605
SNPdbers863223605
MSV3drs863223605
GWAS Ctlgrs863223605
Max Magnitude0
ClinVar
Risk rs863223605(T;T)
Alt rs863223605(T;T)
Reference rs863223605(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN2
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.127670411C>A
CLNSRC
CLNACC RCV000196662.1,