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rs794728187

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728187(G;T)
Make rs794728187(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48497358
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728187
ebirs794728187
HLIrs794728187
Exacrs794728187
Varsomers794728187
Maprs794728187
PheGenIrs794728187
hapmaprs794728187
1000 genomesrs794728187
hgdprs794728187
ensemblrs794728187
gopubmedrs794728187
geneviewrs794728187
scholarrs794728187
googlers794728187
pharmgkbrs794728187
gwascentralrs794728187
openSNPrs794728187
23andMers794728187
23andMe allrs794728187
SNP Nexus

SNPshotrs794728187
SNPdbers794728187
MSV3drs794728187
GWAS Ctlgrs794728187
Max Magnitude0
ClinVar
Risk rs794728187(T;T)
Alt rs794728187(T;T)
Reference rs794728187(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48789555C>A
CLNSRC
CLNACC RCV000181456.1,