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rs730880103

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880103(A;A)
Make rs730880103(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position48460262
GeneFBN1
is asnp
is mentioned by
dbSNPrs730880103
ebirs730880103
HLIrs730880103
Exacrs730880103
Varsomers730880103
Maprs730880103
PheGenIrs730880103
hapmaprs730880103
1000 genomesrs730880103
hgdprs730880103
ensemblrs730880103
gopubmedrs730880103
geneviewrs730880103
scholarrs730880103
googlers730880103
pharmgkbrs730880103
gwascentralrs730880103
openSNPrs730880103
23andMers730880103
23andMe allrs730880103
SNP Nexus

SNPshotrs730880103
SNPdbers730880103
MSV3drs730880103
GWAS Ctlgrs730880103
Max Magnitude0
ClinVar
Risk rs730880103(A;A)
Alt rs730880103(A;A)
Reference rs730880103(T;T)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48752459A>T
CLNSRC
CLNACC RCV000157230.1,