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rs794728274

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728274(A;A)
Make rs794728274(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48421657
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728274
ebirs794728274
HLIrs794728274
Exacrs794728274
Varsomers794728274
Maprs794728274
PheGenIrs794728274
hapmaprs794728274
1000 genomesrs794728274
hgdprs794728274
ensemblrs794728274
gopubmedrs794728274
geneviewrs794728274
scholarrs794728274
googlers794728274
pharmgkbrs794728274
gwascentralrs794728274
openSNPrs794728274
23andMers794728274
23andMe allrs794728274
SNP Nexus

SNPshotrs794728274
SNPdbers794728274
MSV3drs794728274
GWAS Ctlgrs794728274
Max Magnitude0
ClinVar
Risk rs794728274(A;A)
Alt rs794728274(A;A)
Reference rs794728274(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48713854G>T
CLNSRC
CLNACC RCV000181607.1,