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rs794728338

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728338(A;A)
Make rs794728338(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48415710
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728338
ebirs794728338
HLIrs794728338
Exacrs794728338
Varsomers794728338
Maprs794728338
PheGenIrs794728338
hapmaprs794728338
1000 genomesrs794728338
hgdprs794728338
ensemblrs794728338
gopubmedrs794728338
geneviewrs794728338
scholarrs794728338
googlers794728338
pharmgkbrs794728338
gwascentralrs794728338
openSNPrs794728338
23andMers794728338
23andMe allrs794728338
SNP Nexus

SNPshotrs794728338
SNPdbers794728338
MSV3drs794728338
GWAS Ctlgrs794728338
Max Magnitude0
ClinVar
Risk rs794728338(A;A)
Alt rs794728338(A;A)
Reference rs794728338(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48707907A>T
CLNSRC
CLNACC RCV000181707.1,