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rs794728205

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728205(A;A)
Make rs794728205(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48487189
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728205
ebirs794728205
HLIrs794728205
Exacrs794728205
Varsomers794728205
Maprs794728205
PheGenIrs794728205
hapmaprs794728205
1000 genomesrs794728205
hgdprs794728205
ensemblrs794728205
gopubmedrs794728205
geneviewrs794728205
scholarrs794728205
googlers794728205
pharmgkbrs794728205
gwascentralrs794728205
openSNPrs794728205
23andMers794728205
23andMe allrs794728205
SNP Nexus

SNPshotrs794728205
SNPdbers794728205
MSV3drs794728205
GWAS Ctlgrs794728205
Max Magnitude0
ClinVar
Risk rs794728205(A;A)
Alt rs794728205(A;A)
Reference rs794728205(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48779386A>T
CLNSRC
CLNACC RCV000181487.1,