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rs794728181

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728181(A;A)
Make rs794728181(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48503927
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728181
ebirs794728181
HLIrs794728181
Exacrs794728181
Varsomers794728181
Maprs794728181
PheGenIrs794728181
hapmaprs794728181
1000 genomesrs794728181
hgdprs794728181
ensemblrs794728181
gopubmedrs794728181
geneviewrs794728181
scholarrs794728181
googlers794728181
pharmgkbrs794728181
gwascentralrs794728181
openSNPrs794728181
23andMers794728181
23andMe allrs794728181
SNP Nexus

SNPshotrs794728181
SNPdbers794728181
MSV3drs794728181
GWAS Ctlgrs794728181
Max Magnitude0
ClinVar
Risk rs794728181(A;A)
Alt rs794728181(A;A)
Reference rs794728181(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48796124C>T
CLNSRC
CLNACC RCV000181449.1,