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rs794728223

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728223(A;A)
Make rs794728223(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48470646
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728223
ebirs794728223
HLIrs794728223
Exacrs794728223
Varsomers794728223
Maprs794728223
PheGenIrs794728223
hapmaprs794728223
1000 genomesrs794728223
hgdprs794728223
ensemblrs794728223
gopubmedrs794728223
geneviewrs794728223
scholarrs794728223
googlers794728223
pharmgkbrs794728223
gwascentralrs794728223
openSNPrs794728223
23andMers794728223
23andMe allrs794728223
SNP Nexus

SNPshotrs794728223
SNPdbers794728223
MSV3drs794728223
GWAS Ctlgrs794728223
Max Magnitude0
ClinVar
Risk rs794728223(A;A)
Alt rs794728223(A;A)
Reference rs794728223(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48762843C>T
CLNSRC
CLNACC RCV000181521.1,