Have questions? Visit https://www.reddit.com/r/SNPedia

rs794728240

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728240(A;A)
Make rs794728240(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48445492
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728240
ebirs794728240
HLIrs794728240
Exacrs794728240
Varsomers794728240
Maprs794728240
PheGenIrs794728240
hapmaprs794728240
1000 genomesrs794728240
hgdprs794728240
ensemblrs794728240
gopubmedrs794728240
geneviewrs794728240
scholarrs794728240
googlers794728240
pharmgkbrs794728240
gwascentralrs794728240
openSNPrs794728240
23andMers794728240
23andMe allrs794728240
SNP Nexus

SNPshotrs794728240
SNPdbers794728240
MSV3drs794728240
GWAS Ctlgrs794728240
Max Magnitude0
ClinVar
Risk rs794728240(A;A)
Alt rs794728240(A;A)
Reference rs794728240(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48737689C>T
CLNSRC
CLNACC RCV000181552.1,