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rs794728161

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728161(A;A)
Make rs794728161(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48537809
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728161
ebirs794728161
HLIrs794728161
Exacrs794728161
Varsomers794728161
Maprs794728161
PheGenIrs794728161
hapmaprs794728161
1000 genomesrs794728161
hgdprs794728161
ensemblrs794728161
gopubmedrs794728161
geneviewrs794728161
scholarrs794728161
googlers794728161
pharmgkbrs794728161
gwascentralrs794728161
openSNPrs794728161
23andMers794728161
23andMe allrs794728161
SNP Nexus

SNPshotrs794728161
SNPdbers794728161
MSV3drs794728161
GWAS Ctlgrs794728161
Max Magnitude0
ClinVar
Risk rs794728161(A;A)
Alt rs794728161(A;A)
Reference rs794728161(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48830006C>T
CLNSRC
CLNACC RCV000181414.2,