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rs794728322

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728322(C;C)
Make rs794728322(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48494203
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728322
ebirs794728322
HLIrs794728322
Exacrs794728322
Varsomers794728322
Maprs794728322
PheGenIrs794728322
hapmaprs794728322
1000 genomesrs794728322
hgdprs794728322
ensemblrs794728322
gopubmedrs794728322
geneviewrs794728322
scholarrs794728322
googlers794728322
pharmgkbrs794728322
gwascentralrs794728322
openSNPrs794728322
23andMers794728322
23andMe allrs794728322
SNP Nexus

SNPshotrs794728322
SNPdbers794728322
MSV3drs794728322
GWAS Ctlgrs794728322
Max Magnitude0
ClinVar
Risk rs794728322(C;C)
Alt rs794728322(C;C)
Reference rs794728322(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48786400C>G
CLNSRC
CLNACC RCV000181678.1,