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rs794728267

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728267(C;C)
Make rs794728267(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48427639
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728267
ebirs794728267
HLIrs794728267
Exacrs794728267
Varsomers794728267
Maprs794728267
PheGenIrs794728267
hapmaprs794728267
1000 genomesrs794728267
hgdprs794728267
ensemblrs794728267
gopubmedrs794728267
geneviewrs794728267
scholarrs794728267
googlers794728267
pharmgkbrs794728267
gwascentralrs794728267
openSNPrs794728267
23andMers794728267
23andMe allrs794728267
SNP Nexus

SNPshotrs794728267
SNPdbers794728267
MSV3drs794728267
GWAS Ctlgrs794728267
Max Magnitude0
ClinVar
Risk rs794728267(C;C)
Alt rs794728267(C;C)
Reference rs794728267(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48719836A>G
CLNSRC
CLNACC RCV000181594.1,