Have questions? Visit https://www.reddit.com/r/SNPedia

rs863223567

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223567(A;A)
Make rs863223567(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position128338002
GeneFBN2
is asnp
is mentioned by
dbSNPrs863223567
ebirs863223567
HLIrs863223567
Exacrs863223567
Varsomers863223567
Maprs863223567
PheGenIrs863223567
hapmaprs863223567
1000 genomesrs863223567
hgdprs863223567
ensemblrs863223567
gopubmedrs863223567
geneviewrs863223567
scholarrs863223567
googlers863223567
pharmgkbrs863223567
gwascentralrs863223567
openSNPrs863223567
23andMers863223567
23andMe allrs863223567
SNP Nexus

SNPshotrs863223567
SNPdbers863223567
MSV3drs863223567
GWAS Ctlgrs863223567
Max Magnitude0
ClinVar
Risk rs863223567(A;A)
Alt rs863223567(A;A)
Reference rs863223567(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN2
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.127673694C>T
CLNSRC
CLNACC RCV000197367.1,