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rs794728265

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728265(A;A)
Make rs794728265(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48427646
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728265
ebirs794728265
HLIrs794728265
Exacrs794728265
Varsomers794728265
Maprs794728265
PheGenIrs794728265
hapmaprs794728265
1000 genomesrs794728265
hgdprs794728265
ensemblrs794728265
gopubmedrs794728265
geneviewrs794728265
scholarrs794728265
googlers794728265
pharmgkbrs794728265
gwascentralrs794728265
openSNPrs794728265
23andMers794728265
23andMe allrs794728265
SNP Nexus

SNPshotrs794728265
SNPdbers794728265
MSV3drs794728265
GWAS Ctlgrs794728265
Max Magnitude0
ClinVar
Risk rs794728265(A;A)
Alt rs794728265(A;A)
Reference rs794728265(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48719843A>T
CLNSRC
CLNACC RCV000181592.1,