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rs111801777

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs111801777(A;G)
Make rs111801777(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48489875
GeneFBN1
is asnp
is mentioned by
dbSNPrs111801777
ebirs111801777
HLIrs111801777
Exacrs111801777
Varsomers111801777
Maprs111801777
PheGenIrs111801777
hapmaprs111801777
1000 genomesrs111801777
hgdprs111801777
ensemblrs111801777
gopubmedrs111801777
geneviewrs111801777
scholarrs111801777
googlers111801777
pharmgkbrs111801777
gwascentralrs111801777
openSNPrs111801777
23andMers111801777
23andMe allrs111801777
SNP Nexus

SNPshotrs111801777
SNPdbers111801777
MSV3drs111801777
GWAS Ctlgrs111801777
Max Magnitude0
ClinVar
Risk rs111801777(G;G)
Alt rs111801777(G;G)
Reference rs111801777(A;A)
Significance Other
Disease Marfan syndrome not specified Thoracic aortic aneurysm and aortic dissection
Variation info
Gene FBN1
CLNDBN Marfan syndrome not specified Thoracic aortic aneurysm and aortic dissection
Reversed 1
HGVS NC_000015.9:g.48782072T>C
CLNSRC ClinVar University of Washington
CLNACC RCV000035160.5, RCV000161120.4, RCV000227882.1,