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rs794728331

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728331(A;C)
Make rs794728331(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48474641
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728331
ebirs794728331
HLIrs794728331
Exacrs794728331
Varsomers794728331
Maprs794728331
PheGenIrs794728331
hapmaprs794728331
1000 genomesrs794728331
hgdprs794728331
ensemblrs794728331
gopubmedrs794728331
geneviewrs794728331
scholarrs794728331
googlers794728331
pharmgkbrs794728331
gwascentralrs794728331
openSNPrs794728331
23andMers794728331
23andMe allrs794728331
SNP Nexus

SNPshotrs794728331
SNPdbers794728331
MSV3drs794728331
GWAS Ctlgrs794728331
Max Magnitude0
ClinVar
Risk rs794728331(C;C)
Alt rs794728331(C;C)
Reference rs794728331(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48766838T>G
CLNSRC
CLNACC RCV000181692.1,