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rs794728247

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728247(C;C)
Make rs794728247(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48437768
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728247
ebirs794728247
HLIrs794728247
Exacrs794728247
Varsomers794728247
Maprs794728247
PheGenIrs794728247
hapmaprs794728247
1000 genomesrs794728247
hgdprs794728247
ensemblrs794728247
gopubmedrs794728247
geneviewrs794728247
scholarrs794728247
googlers794728247
pharmgkbrs794728247
gwascentralrs794728247
openSNPrs794728247
23andMers794728247
23andMe allrs794728247
SNP Nexus

SNPshotrs794728247
SNPdbers794728247
MSV3drs794728247
GWAS Ctlgrs794728247
Max Magnitude0
ClinVar
Risk rs794728247(C;C)
Alt rs794728247(C;C)
Reference rs794728247(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48729965C>G
CLNSRC
CLNACC RCV000181563.1,