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rs794728211

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728211(G;T)
Make rs794728211(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48481781
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728211
ebirs794728211
HLIrs794728211
Exacrs794728211
Varsomers794728211
Maprs794728211
PheGenIrs794728211
hapmaprs794728211
1000 genomesrs794728211
hgdprs794728211
ensemblrs794728211
gopubmedrs794728211
geneviewrs794728211
scholarrs794728211
googlers794728211
pharmgkbrs794728211
gwascentralrs794728211
openSNPrs794728211
23andMers794728211
23andMe allrs794728211
SNP Nexus

SNPshotrs794728211
SNPdbers794728211
MSV3drs794728211
GWAS Ctlgrs794728211
Max Magnitude0
ClinVar
Risk rs794728211(T;T)
Alt rs794728211(T;T)
Reference rs794728211(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48773978C>A
CLNSRC
CLNACC RCV000181497.1,