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rs794728233

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728233(G;T)
Make rs794728233(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48463943
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728233
ebirs794728233
HLIrs794728233
Exacrs794728233
Varsomers794728233
Maprs794728233
PheGenIrs794728233
hapmaprs794728233
1000 genomesrs794728233
hgdprs794728233
ensemblrs794728233
gopubmedrs794728233
geneviewrs794728233
scholarrs794728233
googlers794728233
pharmgkbrs794728233
gwascentralrs794728233
openSNPrs794728233
23andMers794728233
23andMe allrs794728233
SNP Nexus

SNPshotrs794728233
SNPdbers794728233
MSV3drs794728233
GWAS Ctlgrs794728233
Max Magnitude0
ClinVar
Risk rs794728233(T;T)
Alt rs794728233(T;T)
Reference rs794728233(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48756140C>A
CLNSRC
CLNACC RCV000181537.2,