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rs794728228

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728228(C;T)
Make rs794728228(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48468064
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728228
ebirs794728228
HLIrs794728228
Exacrs794728228
Varsomers794728228
Maprs794728228
PheGenIrs794728228
hapmaprs794728228
1000 genomesrs794728228
hgdprs794728228
ensemblrs794728228
gopubmedrs794728228
geneviewrs794728228
scholarrs794728228
googlers794728228
pharmgkbrs794728228
gwascentralrs794728228
openSNPrs794728228
23andMers794728228
23andMe allrs794728228
SNP Nexus

SNPshotrs794728228
SNPdbers794728228
MSV3drs794728228
GWAS Ctlgrs794728228
Max Magnitude0
ClinVar
Risk rs794728228(T;T)
Alt rs794728228(T;T)
Reference rs794728228(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48760261G>A
CLNSRC
CLNACC RCV000181529.2,