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rs863223570

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223570(C;C)
Make rs863223570(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position128335986
GeneFBN2
is asnp
is mentioned by
dbSNPrs863223570
ebirs863223570
HLIrs863223570
Exacrs863223570
Varsomers863223570
Maprs863223570
PheGenIrs863223570
hapmaprs863223570
1000 genomesrs863223570
hgdprs863223570
ensemblrs863223570
gopubmedrs863223570
geneviewrs863223570
scholarrs863223570
googlers863223570
pharmgkbrs863223570
gwascentralrs863223570
openSNPrs863223570
23andMers863223570
23andMe allrs863223570
SNP Nexus

SNPshotrs863223570
SNPdbers863223570
MSV3drs863223570
GWAS Ctlgrs863223570
Max Magnitude0
ClinVar
Risk rs863223570(C;C)
Alt rs863223570(C;C)
Reference rs863223570(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN2
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.127671678A>G
CLNSRC
CLNACC RCV000199998.1,