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rs794728253

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728253(C;C)
Make rs794728253(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48432977
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728253
ebirs794728253
HLIrs794728253
Exacrs794728253
Varsomers794728253
Maprs794728253
PheGenIrs794728253
hapmaprs794728253
1000 genomesrs794728253
hgdprs794728253
ensemblrs794728253
gopubmedrs794728253
geneviewrs794728253
scholarrs794728253
googlers794728253
pharmgkbrs794728253
gwascentralrs794728253
openSNPrs794728253
23andMers794728253
23andMe allrs794728253
SNP Nexus

SNPshotrs794728253
SNPdbers794728253
MSV3drs794728253
GWAS Ctlgrs794728253
Max Magnitude0
ClinVar
Risk rs794728253(C;C)
Alt rs794728253(C;C)
Reference rs794728253(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48725174A>G
CLNSRC
CLNACC RCV000181572.2,