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rs794728336

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728336(A;G)
Make rs794728336(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48421680
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728336
ebirs794728336
HLIrs794728336
Exacrs794728336
Varsomers794728336
Maprs794728336
PheGenIrs794728336
hapmaprs794728336
1000 genomesrs794728336
hgdprs794728336
ensemblrs794728336
gopubmedrs794728336
geneviewrs794728336
scholarrs794728336
googlers794728336
pharmgkbrs794728336
gwascentralrs794728336
openSNPrs794728336
23andMers794728336
23andMe allrs794728336
SNP Nexus

SNPshotrs794728336
SNPdbers794728336
MSV3drs794728336
GWAS Ctlgrs794728336
Max Magnitude0
ClinVar
Risk rs794728336(G;G)
Alt rs794728336(G;G)
Reference rs794728336(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene FBN1
CLNDBN not specified
Reversed 1
HGVS NC_000015.9:g.48713877T>C
CLNSRC
CLNACC RCV000181705.2,