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rs794728327

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728327(A;A)
Make rs794728327(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48497261
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728327
ebirs794728327
HLIrs794728327
Exacrs794728327
Varsomers794728327
Maprs794728327
PheGenIrs794728327
hapmaprs794728327
1000 genomesrs794728327
hgdprs794728327
ensemblrs794728327
gopubmedrs794728327
geneviewrs794728327
scholarrs794728327
googlers794728327
pharmgkbrs794728327
gwascentralrs794728327
openSNPrs794728327
23andMers794728327
23andMe allrs794728327
SNP Nexus

SNPshotrs794728327
SNPdbers794728327
MSV3drs794728327
GWAS Ctlgrs794728327
Max Magnitude0
ClinVar
Risk rs794728327(A;A)
Alt rs794728327(A;A)
Reference rs794728327(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48789458C>T
CLNSRC
CLNACC RCV000181686.1,