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rs794728212

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728212(A;A)
Make rs794728212(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48481654
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728212
ebirs794728212
HLIrs794728212
Exacrs794728212
Varsomers794728212
Maprs794728212
PheGenIrs794728212
hapmaprs794728212
1000 genomesrs794728212
hgdprs794728212
ensemblrs794728212
gopubmedrs794728212
geneviewrs794728212
scholarrs794728212
googlers794728212
pharmgkbrs794728212
gwascentralrs794728212
openSNPrs794728212
23andMers794728212
23andMe allrs794728212
SNP Nexus

SNPshotrs794728212
SNPdbers794728212
MSV3drs794728212
GWAS Ctlgrs794728212
Max Magnitude0
ClinVar
Risk rs794728212(A;A)
Alt rs794728212(A;A)
Reference rs794728212(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48773851C>T
CLNSRC
CLNACC RCV000181500.1,