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rs794728249

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728249(A;A)
Make rs794728249(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48437039
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728249
ebirs794728249
HLIrs794728249
Exacrs794728249
Varsomers794728249
Maprs794728249
PheGenIrs794728249
hapmaprs794728249
1000 genomesrs794728249
hgdprs794728249
ensemblrs794728249
gopubmedrs794728249
geneviewrs794728249
scholarrs794728249
googlers794728249
pharmgkbrs794728249
gwascentralrs794728249
openSNPrs794728249
23andMers794728249
23andMe allrs794728249
SNP Nexus

SNPshotrs794728249
SNPdbers794728249
MSV3drs794728249
GWAS Ctlgrs794728249
Max Magnitude0
ClinVar
Risk rs794728249(A;A)
Alt rs794728249(A;A)
Reference rs794728249(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48729236C>T
CLNSRC
CLNACC RCV000181566.1,