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rs730880107

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880107(A;A)
Make rs730880107(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position48432864
GeneFBN1
is asnp
is mentioned by
dbSNPrs730880107
ebirs730880107
HLIrs730880107
Exacrs730880107
Varsomers730880107
Maprs730880107
PheGenIrs730880107
hapmaprs730880107
1000 genomesrs730880107
hgdprs730880107
ensemblrs730880107
gopubmedrs730880107
geneviewrs730880107
scholarrs730880107
googlers730880107
pharmgkbrs730880107
gwascentralrs730880107
openSNPrs730880107
23andMers730880107
23andMe allrs730880107
SNP Nexus

SNPshotrs730880107
SNPdbers730880107
MSV3drs730880107
GWAS Ctlgrs730880107
Max Magnitude0
ClinVar
Risk rs730880107(A;A)
Alt rs730880107(A;A)
Reference rs730880107(T;T)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48725061A>T
CLNSRC
CLNACC RCV000157234.1,