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rs794728166

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728166(A;A)
Make rs794728166(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48515434
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728166
ebirs794728166
HLIrs794728166
Exacrs794728166
Varsomers794728166
Maprs794728166
PheGenIrs794728166
hapmaprs794728166
1000 genomesrs794728166
hgdprs794728166
ensemblrs794728166
gopubmedrs794728166
geneviewrs794728166
scholarrs794728166
googlers794728166
pharmgkbrs794728166
gwascentralrs794728166
openSNPrs794728166
23andMers794728166
23andMe allrs794728166
SNP Nexus

SNPshotrs794728166
SNPdbers794728166
MSV3drs794728166
GWAS Ctlgrs794728166
Max Magnitude0
ClinVar
Risk rs794728166(A;A)
Alt rs794728166(A;A)
Reference rs794728166(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48807631C>T
CLNSRC
CLNACC RCV000181428.2,