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rs730880098

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880098(G;T)
Make rs730880098(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position48610793
GeneFBN1
is asnp
is mentioned by
dbSNPrs730880098
dbSNP (old)rs730880098
ClinGenrs730880098
ebirs730880098
HLIrs730880098
Exacrs730880098
Gnomadrs730880098
Varsomers730880098
Maprs730880098
PheGenIrs730880098
Biobankrs730880098
1000 genomesrs730880098
hgdprs730880098
ensemblrs730880098
gopubmedrs730880098
geneviewrs730880098
scholarrs730880098
googlers730880098
pharmgkbrs730880098
gwascentralrs730880098
openSNPrs730880098
23andMers730880098
23andMe allrs730880098
SNP Nexus

SNPshotrs730880098
SNPdbers730880098
MSV3drs730880098
GWAS Ctlgrs730880098
Max Magnitude0
ClinVar
Risk rs730880098(T;T)
Alt rs730880098(T;T)
Reference Rs730880098(G;G)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48902990C>A
CLNSRC
CLNACC RCV000157223.1,