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rs794728218

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728218(A;A)
Make rs794728218(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48474319
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728218
ebirs794728218
HLIrs794728218
Exacrs794728218
Varsomers794728218
Maprs794728218
PheGenIrs794728218
hapmaprs794728218
1000 genomesrs794728218
hgdprs794728218
ensemblrs794728218
gopubmedrs794728218
geneviewrs794728218
scholarrs794728218
googlers794728218
pharmgkbrs794728218
gwascentralrs794728218
openSNPrs794728218
23andMers794728218
23andMe allrs794728218
SNP Nexus

SNPshotrs794728218
SNPdbers794728218
MSV3drs794728218
GWAS Ctlgrs794728218
Max Magnitude0
ClinVar
Risk rs794728218(A;A)
Alt rs794728218(A;A)
Reference rs794728218(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48766516A>T
CLNSRC
CLNACC RCV000181509.1,