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rs863223604

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223604(G;T)
Make rs863223604(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position128335454
GeneFBN2
is asnp
is mentioned by
dbSNPrs863223604
ebirs863223604
HLIrs863223604
Exacrs863223604
Varsomers863223604
Maprs863223604
PheGenIrs863223604
hapmaprs863223604
1000 genomesrs863223604
hgdprs863223604
ensemblrs863223604
gopubmedrs863223604
geneviewrs863223604
scholarrs863223604
googlers863223604
pharmgkbrs863223604
gwascentralrs863223604
openSNPrs863223604
23andMers863223604
23andMe allrs863223604
SNP Nexus

SNPshotrs863223604
SNPdbers863223604
MSV3drs863223604
GWAS Ctlgrs863223604
Max Magnitude0
ClinVar
Risk rs863223604(T;T)
Alt rs863223604(T;T)
Reference rs863223604(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN2
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.127671146C>A
CLNSRC
CLNACC RCV000196708.1,