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rs794728210

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728210(A;A)
Make rs794728210(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48483818
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728210
ebirs794728210
HLIrs794728210
Exacrs794728210
Varsomers794728210
Maprs794728210
PheGenIrs794728210
hapmaprs794728210
1000 genomesrs794728210
hgdprs794728210
ensemblrs794728210
gopubmedrs794728210
geneviewrs794728210
scholarrs794728210
googlers794728210
pharmgkbrs794728210
gwascentralrs794728210
openSNPrs794728210
23andMers794728210
23andMe allrs794728210
SNP Nexus

SNPshotrs794728210
SNPdbers794728210
MSV3drs794728210
GWAS Ctlgrs794728210
Max Magnitude0
ClinVar
Risk rs794728210(A;A)
Alt rs794728210(A;A)
Reference rs794728210(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48776015C>T
CLNSRC
CLNACC RCV000181496.1,