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rs794728292

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728292(G;T)
Make rs794728292(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48610769
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728292
ebirs794728292
HLIrs794728292
Exacrs794728292
Varsomers794728292
Maprs794728292
PheGenIrs794728292
hapmaprs794728292
1000 genomesrs794728292
hgdprs794728292
ensemblrs794728292
gopubmedrs794728292
geneviewrs794728292
scholarrs794728292
googlers794728292
pharmgkbrs794728292
gwascentralrs794728292
openSNPrs794728292
23andMers794728292
23andMe allrs794728292
SNP Nexus

SNPshotrs794728292
SNPdbers794728292
MSV3drs794728292
GWAS Ctlgrs794728292
Max Magnitude0
ClinVar
Risk rs794728292(T;T)
Alt rs794728292(T;T)
Reference rs794728292(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48902966C>A
CLNSRC
CLNACC RCV000181645.1,