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rs794728277

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728277(A;A)
Make rs794728277(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48420731
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728277
ebirs794728277
HLIrs794728277
Exacrs794728277
Varsomers794728277
Maprs794728277
PheGenIrs794728277
hapmaprs794728277
1000 genomesrs794728277
hgdprs794728277
ensemblrs794728277
gopubmedrs794728277
geneviewrs794728277
scholarrs794728277
googlers794728277
pharmgkbrs794728277
gwascentralrs794728277
openSNPrs794728277
23andMers794728277
23andMe allrs794728277
SNP Nexus

SNPshotrs794728277
SNPdbers794728277
MSV3drs794728277
GWAS Ctlgrs794728277
Max Magnitude0
ClinVar
Risk rs794728277(A;A)
Alt rs794728277(A;A)
Reference rs794728277(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48712928C>T
CLNSRC
CLNACC RCV000181614.2,