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rs794728186

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728186(A;A)
Make rs794728186(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48497379
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728186
ebirs794728186
HLIrs794728186
Exacrs794728186
Varsomers794728186
Maprs794728186
PheGenIrs794728186
hapmaprs794728186
1000 genomesrs794728186
hgdprs794728186
ensemblrs794728186
gopubmedrs794728186
geneviewrs794728186
scholarrs794728186
googlers794728186
pharmgkbrs794728186
gwascentralrs794728186
openSNPrs794728186
23andMers794728186
23andMe allrs794728186
SNP Nexus

SNPshotrs794728186
SNPdbers794728186
MSV3drs794728186
GWAS Ctlgrs794728186
Max Magnitude0
ClinVar
Risk rs794728186(A;A)
Alt rs794728186(A;A)
Reference rs794728186(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48789576C>T
CLNSRC
CLNACC RCV000181455.1,