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

rs794728270

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728270(A;A)
Make rs794728270(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48425816
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728270
ebirs794728270
HLIrs794728270
Exacrs794728270
Varsomers794728270
Maprs794728270
PheGenIrs794728270
hapmaprs794728270
1000 genomesrs794728270
hgdprs794728270
ensemblrs794728270
gopubmedrs794728270
geneviewrs794728270
scholarrs794728270
googlers794728270
pharmgkbrs794728270
gwascentralrs794728270
openSNPrs794728270
23andMers794728270
23andMe allrs794728270
SNP Nexus

SNPshotrs794728270
SNPdbers794728270
MSV3drs794728270
GWAS Ctlgrs794728270
Max Magnitude0
ClinVar
Risk rs794728270(A;A)
Alt rs794728270(A;A)
Reference rs794728270(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48718013C>T
CLNSRC
CLNACC RCV000181597.2,