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rs794728291

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728291(C;C)
Make rs794728291(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48610787
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728291
ebirs794728291
HLIrs794728291
Exacrs794728291
Varsomers794728291
Maprs794728291
PheGenIrs794728291
hapmaprs794728291
1000 genomesrs794728291
hgdprs794728291
ensemblrs794728291
gopubmedrs794728291
geneviewrs794728291
scholarrs794728291
googlers794728291
pharmgkbrs794728291
gwascentralrs794728291
openSNPrs794728291
23andMers794728291
23andMe allrs794728291
SNP Nexus

SNPshotrs794728291
SNPdbers794728291
MSV3drs794728291
GWAS Ctlgrs794728291
Max Magnitude0
ClinVar
Risk rs794728291(C;C)
Alt rs794728291(C;C)
Reference rs794728291(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48902984C>G
CLNSRC
CLNACC RCV000181644.1,