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rs794728197

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728197(C;T)
Make rs794728197(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48492509
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728197
ebirs794728197
HLIrs794728197
Exacrs794728197
Varsomers794728197
Maprs794728197
PheGenIrs794728197
hapmaprs794728197
1000 genomesrs794728197
hgdprs794728197
ensemblrs794728197
gopubmedrs794728197
geneviewrs794728197
scholarrs794728197
googlers794728197
pharmgkbrs794728197
gwascentralrs794728197
openSNPrs794728197
23andMers794728197
23andMe allrs794728197
SNP Nexus

SNPshotrs794728197
SNPdbers794728197
MSV3drs794728197
GWAS Ctlgrs794728197
Max Magnitude0
ClinVar
Risk rs794728197(T;T)
Alt rs794728197(T;T)
Reference rs794728197(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48784706G>A
CLNSRC
CLNACC RCV000181467.2,