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rs794728334

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728334(A;A)
Make rs794728334(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48437069
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728334
ebirs794728334
HLIrs794728334
Exacrs794728334
Varsomers794728334
Maprs794728334
PheGenIrs794728334
hapmaprs794728334
1000 genomesrs794728334
hgdprs794728334
ensemblrs794728334
gopubmedrs794728334
geneviewrs794728334
scholarrs794728334
googlers794728334
pharmgkbrs794728334
gwascentralrs794728334
openSNPrs794728334
23andMers794728334
23andMe allrs794728334
SNP Nexus

SNPshotrs794728334
SNPdbers794728334
MSV3drs794728334
GWAS Ctlgrs794728334
Max Magnitude0
ClinVar
Risk rs794728334(A;A)
Alt rs794728334(A;A)
Reference rs794728334(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48729266C>T
CLNSRC
CLNACC RCV000181698.1,