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rs794728192

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728192(A;A)
Make rs794728192(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48495468
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728192
ebirs794728192
HLIrs794728192
Exacrs794728192
Varsomers794728192
Maprs794728192
PheGenIrs794728192
hapmaprs794728192
1000 genomesrs794728192
hgdprs794728192
ensemblrs794728192
gopubmedrs794728192
geneviewrs794728192
scholarrs794728192
googlers794728192
pharmgkbrs794728192
gwascentralrs794728192
openSNPrs794728192
23andMers794728192
23andMe allrs794728192
SNP Nexus

SNPshotrs794728192
SNPdbers794728192
MSV3drs794728192
GWAS Ctlgrs794728192
Max Magnitude0
ClinVar
Risk rs794728192(A;A)
Alt rs794728192(A;A)
Reference rs794728192(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48787665C>T
CLNSRC
CLNACC RCV000181462.1,