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rs794728342

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794728342(-;G)
Make rs794728342(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48487373
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728342
ClinGenrs794728342
ebirs794728342
HLIrs794728342
Exacrs794728342
Varsomers794728342
Maprs794728342
PheGenIrs794728342
hapmaprs794728342
1000 genomesrs794728342
hgdprs794728342
ensemblrs794728342
gopubmedrs794728342
geneviewrs794728342
scholarrs794728342
googlers794728342
pharmgkbrs794728342
gwascentralrs794728342
openSNPrs794728342
23andMers794728342
23andMe allrs794728342
SNP Nexus

SNPshotrs794728342
SNPdbers794728342
MSV3drs794728342
GWAS Ctlgrs794728342
Max Magnitude0
ClinVar
Risk rs794728342(G;G)
Alt rs794728342(G;G)
Reference Rs794728342(;)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48779571dupC
CLNSRC
CLNACC RCV000181712.2,