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rs794728337

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728337(A;A)
Make rs794728337(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48415755
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728337
ebirs794728337
HLIrs794728337
Exacrs794728337
Varsomers794728337
Maprs794728337
PheGenIrs794728337
hapmaprs794728337
1000 genomesrs794728337
hgdprs794728337
ensemblrs794728337
gopubmedrs794728337
geneviewrs794728337
scholarrs794728337
googlers794728337
pharmgkbrs794728337
gwascentralrs794728337
openSNPrs794728337
23andMers794728337
23andMe allrs794728337
SNP Nexus

SNPshotrs794728337
SNPdbers794728337
MSV3drs794728337
GWAS Ctlgrs794728337
Max Magnitude0
ClinVar
Risk rs794728337(A;A)
Alt rs794728337(A;A)
Reference rs794728337(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48707952C>T
CLNSRC
CLNACC RCV000181706.2,