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

rs794728217

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728217(A;G)
Make rs794728217(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48474371
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728217
ebirs794728217
HLIrs794728217
Exacrs794728217
Varsomers794728217
Maprs794728217
PheGenIrs794728217
hapmaprs794728217
1000 genomesrs794728217
hgdprs794728217
ensemblrs794728217
gopubmedrs794728217
geneviewrs794728217
scholarrs794728217
googlers794728217
pharmgkbrs794728217
gwascentralrs794728217
openSNPrs794728217
23andMers794728217
23andMe allrs794728217
SNP Nexus

SNPshotrs794728217
SNPdbers794728217
MSV3drs794728217
GWAS Ctlgrs794728217
Max Magnitude0
ClinVar
Risk rs794728217(G;G)
Alt rs794728217(G;G)
Reference rs794728217(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48766568T>C
CLNSRC
CLNACC RCV000181507.2,