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rs794728216

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728216(A;G)
Make rs794728216(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48470758
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728216
ebirs794728216
HLIrs794728216
Exacrs794728216
Varsomers794728216
Maprs794728216
PheGenIrs794728216
hapmaprs794728216
1000 genomesrs794728216
hgdprs794728216
ensemblrs794728216
gopubmedrs794728216
geneviewrs794728216
scholarrs794728216
googlers794728216
pharmgkbrs794728216
gwascentralrs794728216
openSNPrs794728216
23andMers794728216
23andMe allrs794728216
SNP Nexus

SNPshotrs794728216
SNPdbers794728216
MSV3drs794728216
GWAS Ctlgrs794728216
Max Magnitude0
ClinVar
Risk rs794728216(G;G)
Alt rs794728216(G;G)
Reference rs794728216(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48762955T>C
CLNSRC
CLNACC RCV000181506.1,