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

rs368439899

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs368439899(A;A)
Make rs368439899(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48432898
GeneFBN1
is asnp
is mentioned by
dbSNPrs368439899
ebirs368439899
HLIrs368439899
Exacrs368439899
Varsomers368439899
Maprs368439899
PheGenIrs368439899
hapmaprs368439899
1000 genomesrs368439899
hgdprs368439899
ensemblrs368439899
gopubmedrs368439899
geneviewrs368439899
scholarrs368439899
googlers368439899
pharmgkbrs368439899
gwascentralrs368439899
openSNPrs368439899
23andMers368439899
23andMe allrs368439899
SNP Nexus

SNPshotrs368439899
SNPdbers368439899
MSV3drs368439899
GWAS Ctlgrs368439899
Max Magnitude0
ClinVar
Risk rs368439899(A;A)
Alt rs368439899(A;A)
Reference rs368439899(T;T)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene FBN1
CLNDBN not specified
Reversed 0
HGVS NC_000015.9:g.48725095T>A
CLNSRC
CLNACC RCV000181578.2,