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rs794728325

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728325(A;A)
Make rs794728325(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48520659
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728325
ebirs794728325
HLIrs794728325
Exacrs794728325
Varsomers794728325
Maprs794728325
PheGenIrs794728325
hapmaprs794728325
1000 genomesrs794728325
hgdprs794728325
ensemblrs794728325
gopubmedrs794728325
geneviewrs794728325
scholarrs794728325
googlers794728325
pharmgkbrs794728325
gwascentralrs794728325
openSNPrs794728325
23andMers794728325
23andMe allrs794728325
SNP Nexus

SNPshotrs794728325
SNPdbers794728325
MSV3drs794728325
GWAS Ctlgrs794728325
Max Magnitude0
ClinVar
Risk rs794728325(A;A)
Alt rs794728325(A;A)
Reference rs794728325(G;G)
Significance Probable-Pathogenic
Disease not specified Marfan syndrome
Variation info
Gene FBN1
CLNDBN not specified Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48812856C>T
CLNSRC
CLNACC RCV000181682.2, RCV000231553.1,