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rs794728220

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728220(A;A)
Make rs794728220(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48474255
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728220
ebirs794728220
HLIrs794728220
Exacrs794728220
Varsomers794728220
Maprs794728220
PheGenIrs794728220
hapmaprs794728220
1000 genomesrs794728220
hgdprs794728220
ensemblrs794728220
gopubmedrs794728220
geneviewrs794728220
scholarrs794728220
googlers794728220
pharmgkbrs794728220
gwascentralrs794728220
openSNPrs794728220
23andMers794728220
23andMe allrs794728220
SNP Nexus

SNPshotrs794728220
SNPdbers794728220
MSV3drs794728220
GWAS Ctlgrs794728220
Max Magnitude0
ClinVar
Risk rs794728220(A;A)
Alt rs794728220(A;A)
Reference rs794728220(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48766452C>T
CLNSRC
CLNACC RCV000181512.1,