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rs794728204

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728204(A;A)
Make rs794728204(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48487312
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728204
ebirs794728204
HLIrs794728204
Exacrs794728204
Varsomers794728204
Maprs794728204
PheGenIrs794728204
hapmaprs794728204
1000 genomesrs794728204
hgdprs794728204
ensemblrs794728204
gopubmedrs794728204
geneviewrs794728204
scholarrs794728204
googlers794728204
pharmgkbrs794728204
gwascentralrs794728204
openSNPrs794728204
23andMers794728204
23andMe allrs794728204
SNP Nexus

SNPshotrs794728204
SNPdbers794728204
MSV3drs794728204
GWAS Ctlgrs794728204
Max Magnitude0
ClinVar
Risk rs794728204(A;A)
Alt rs794728204(A;A)
Reference rs794728204(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48779509C>T
CLNSRC
CLNACC RCV000181486.2,