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rs794728190

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728190(A;A)
Make rs794728190(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48496213
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728190
ebirs794728190
HLIrs794728190
Exacrs794728190
Varsomers794728190
Maprs794728190
PheGenIrs794728190
hapmaprs794728190
1000 genomesrs794728190
hgdprs794728190
ensemblrs794728190
gopubmedrs794728190
geneviewrs794728190
scholarrs794728190
googlers794728190
pharmgkbrs794728190
gwascentralrs794728190
openSNPrs794728190
23andMers794728190
23andMe allrs794728190
SNP Nexus

SNPshotrs794728190
SNPdbers794728190
MSV3drs794728190
GWAS Ctlgrs794728190
Max Magnitude0
ClinVar
Risk rs794728190(A;A)
Alt rs794728190(A;A)
Reference rs794728190(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48788410C>T
CLNSRC
CLNACC RCV000181459.2,