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rs794728326

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728326(G;G)
Make rs794728326(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48515429
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728326
ebirs794728326
HLIrs794728326
Exacrs794728326
Varsomers794728326
Maprs794728326
PheGenIrs794728326
hapmaprs794728326
1000 genomesrs794728326
hgdprs794728326
ensemblrs794728326
gopubmedrs794728326
geneviewrs794728326
scholarrs794728326
googlers794728326
pharmgkbrs794728326
gwascentralrs794728326
openSNPrs794728326
23andMers794728326
23andMe allrs794728326
SNP Nexus

SNPshotrs794728326
SNPdbers794728326
MSV3drs794728326
GWAS Ctlgrs794728326
Max Magnitude0
ClinVar
Risk rs794728326(G;G)
Alt rs794728326(G;G)
Reference rs794728326(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48807626A>C
CLNSRC
CLNACC RCV000181684.1,