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rs727505110

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727505110(C;C)
Make rs727505110(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position48489991
GeneFBN1
is asnp
is mentioned by
dbSNPrs727505110
ebirs727505110
HLIrs727505110
Exacrs727505110
Varsomers727505110
Maprs727505110
PheGenIrs727505110
hapmaprs727505110
1000 genomesrs727505110
hgdprs727505110
ensemblrs727505110
gopubmedrs727505110
geneviewrs727505110
scholarrs727505110
googlers727505110
pharmgkbrs727505110
gwascentralrs727505110
openSNPrs727505110
23andMers727505110
23andMe allrs727505110
SNP Nexus

SNPshotrs727505110
SNPdbers727505110
MSV3drs727505110
GWAS Ctlgrs727505110
Max Magnitude0
ClinVar
Risk rs727505110(C;C)
Alt rs727505110(C;C)
Reference rs727505110(G;G)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48782188C>G
CLNSRC
CLNACC RCV000156563.1,