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rs794728272

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728272(C;C)
Make rs794728272(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48421991
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728272
ebirs794728272
HLIrs794728272
Exacrs794728272
Varsomers794728272
Maprs794728272
PheGenIrs794728272
hapmaprs794728272
1000 genomesrs794728272
hgdprs794728272
ensemblrs794728272
gopubmedrs794728272
geneviewrs794728272
scholarrs794728272
googlers794728272
pharmgkbrs794728272
gwascentralrs794728272
openSNPrs794728272
23andMers794728272
23andMe allrs794728272
SNP Nexus

SNPshotrs794728272
SNPdbers794728272
MSV3drs794728272
GWAS Ctlgrs794728272
Max Magnitude0
ClinVar
Risk rs794728272(C;C)
Alt rs794728272(C;C)
Reference rs794728272(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48714188A>G
CLNSRC
CLNACC RCV000181605.1,