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rs794728281

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728281(G;T)
Make rs794728281(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48415582
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728281
ebirs794728281
HLIrs794728281
Exacrs794728281
Varsomers794728281
Maprs794728281
PheGenIrs794728281
hapmaprs794728281
1000 genomesrs794728281
hgdprs794728281
ensemblrs794728281
gopubmedrs794728281
geneviewrs794728281
scholarrs794728281
googlers794728281
pharmgkbrs794728281
gwascentralrs794728281
openSNPrs794728281
23andMers794728281
23andMe allrs794728281
SNP Nexus

SNPshotrs794728281
SNPdbers794728281
MSV3drs794728281
GWAS Ctlgrs794728281
Max Magnitude0
ClinVar
Risk rs794728281(T;T)
Alt rs794728281(T;T)
Reference rs794728281(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48707779C>A
CLNSRC
CLNACC RCV000181623.2,