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rs794728283

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728283(C;T)
Make rs794728283(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48415549
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728283
ebirs794728283
HLIrs794728283
Exacrs794728283
Varsomers794728283
Maprs794728283
PheGenIrs794728283
hapmaprs794728283
1000 genomesrs794728283
hgdprs794728283
ensemblrs794728283
gopubmedrs794728283
geneviewrs794728283
scholarrs794728283
googlers794728283
pharmgkbrs794728283
gwascentralrs794728283
openSNPrs794728283
23andMers794728283
23andMe allrs794728283
SNP Nexus

SNPshotrs794728283
SNPdbers794728283
MSV3drs794728283
GWAS Ctlgrs794728283
Max Magnitude0
ClinVar
Risk rs794728283(T;T)
Alt rs794728283(T;T)
Reference rs794728283(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48707746G>A
CLNSRC
CLNACC RCV000181625.2,