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rs794728269

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728269(A;A)
Make rs794728269(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48425823
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728269
ebirs794728269
HLIrs794728269
Exacrs794728269
Varsomers794728269
Maprs794728269
PheGenIrs794728269
hapmaprs794728269
1000 genomesrs794728269
hgdprs794728269
ensemblrs794728269
gopubmedrs794728269
geneviewrs794728269
scholarrs794728269
googlers794728269
pharmgkbrs794728269
gwascentralrs794728269
openSNPrs794728269
23andMers794728269
23andMe allrs794728269
SNP Nexus

SNPshotrs794728269
SNPdbers794728269
MSV3drs794728269
GWAS Ctlgrs794728269
Max Magnitude0
ClinVar
Risk rs794728269(A;A)
Alt rs794728269(A;A)
Reference rs794728269(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48718020C>T
CLNSRC
CLNACC RCV000181596.2,