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rs794728264

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728264(C;C)
Make rs794728264(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48427660
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728264
ebirs794728264
HLIrs794728264
Exacrs794728264
Varsomers794728264
Maprs794728264
PheGenIrs794728264
hapmaprs794728264
1000 genomesrs794728264
hgdprs794728264
ensemblrs794728264
gopubmedrs794728264
geneviewrs794728264
scholarrs794728264
googlers794728264
pharmgkbrs794728264
gwascentralrs794728264
openSNPrs794728264
23andMers794728264
23andMe allrs794728264
SNP Nexus

SNPshotrs794728264
SNPdbers794728264
MSV3drs794728264
GWAS Ctlgrs794728264
Max Magnitude0
ClinVar
Risk rs794728264(C;C)
Alt rs794728264(C;C)
Reference rs794728264(T;T)
Significance Pathogenic
Disease not specified
Variation info
Gene FBN1
CLNDBN not specified
Reversed 1
HGVS NC_000015.9:g.48719857A>G
CLNSRC
CLNACC RCV000181591.3,