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rs794728200

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728200(G;G)
Make rs794728200(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48489913
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728200
ebirs794728200
HLIrs794728200
Exacrs794728200
Varsomers794728200
Maprs794728200
PheGenIrs794728200
hapmaprs794728200
1000 genomesrs794728200
hgdprs794728200
ensemblrs794728200
gopubmedrs794728200
geneviewrs794728200
scholarrs794728200
googlers794728200
pharmgkbrs794728200
gwascentralrs794728200
openSNPrs794728200
23andMers794728200
23andMe allrs794728200
SNP Nexus

SNPshotrs794728200
SNPdbers794728200
MSV3drs794728200
GWAS Ctlgrs794728200
Max Magnitude0
ClinVar
Risk rs794728200(G;G)
Alt rs794728200(G;G)
Reference rs794728200(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48782110A>C
CLNSRC
CLNACC RCV000181475.2,