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rs794728246

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728246(C;C)
Make rs794728246(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48437807
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728246
ebirs794728246
HLIrs794728246
Exacrs794728246
Varsomers794728246
Maprs794728246
PheGenIrs794728246
hapmaprs794728246
1000 genomesrs794728246
hgdprs794728246
ensemblrs794728246
gopubmedrs794728246
geneviewrs794728246
scholarrs794728246
googlers794728246
pharmgkbrs794728246
gwascentralrs794728246
openSNPrs794728246
23andMers794728246
23andMe allrs794728246
SNP Nexus

SNPshotrs794728246
SNPdbers794728246
MSV3drs794728246
GWAS Ctlgrs794728246
Max Magnitude0
ClinVar
Risk rs794728246(C;C)
Alt rs794728246(C;C)
Reference rs794728246(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48730004A>G
CLNSRC
CLNACC RCV000181562.1,