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rs794728236

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728236(A;A)
Make rs794728236(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48446794
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728236
ebirs794728236
HLIrs794728236
Exacrs794728236
Varsomers794728236
Maprs794728236
PheGenIrs794728236
hapmaprs794728236
1000 genomesrs794728236
hgdprs794728236
ensemblrs794728236
gopubmedrs794728236
geneviewrs794728236
scholarrs794728236
googlers794728236
pharmgkbrs794728236
gwascentralrs794728236
openSNPrs794728236
23andMers794728236
23andMe allrs794728236
SNP Nexus

SNPshotrs794728236
SNPdbers794728236
MSV3drs794728236
GWAS Ctlgrs794728236
Max Magnitude0
ClinVar
Risk rs794728236(A;A)
Alt rs794728236(A;A)
Reference rs794728236(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48738991A>T
CLNSRC
CLNACC RCV000181542.1,