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rs794728282

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728282(C;G)
Make rs794728282(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48415577
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728282
ebirs794728282
HLIrs794728282
Exacrs794728282
Varsomers794728282
Maprs794728282
PheGenIrs794728282
hapmaprs794728282
1000 genomesrs794728282
hgdprs794728282
ensemblrs794728282
gopubmedrs794728282
geneviewrs794728282
scholarrs794728282
googlers794728282
pharmgkbrs794728282
gwascentralrs794728282
openSNPrs794728282
23andMers794728282
23andMe allrs794728282
SNP Nexus

SNPshotrs794728282
SNPdbers794728282
MSV3drs794728282
GWAS Ctlgrs794728282
Max Magnitude0
ClinVar
Risk rs794728282(G;G)
Alt rs794728282(G;G)
Reference rs794728282(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48707774G>C
CLNSRC
CLNACC RCV000181624.1,