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rs267606797

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606797(G;G)
Make rs267606797(G;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position48437362
GeneFBN1
is asnp
is mentioned by
dbSNPrs267606797
ebirs267606797
HLIrs267606797
Exacrs267606797
Varsomers267606797
Maprs267606797
PheGenIrs267606797
hapmaprs267606797
1000 genomesrs267606797
hgdprs267606797
ensemblrs267606797
gopubmedrs267606797
geneviewrs267606797
scholarrs267606797
googlers267606797
pharmgkbrs267606797
gwascentralrs267606797
openSNPrs267606797
23andMers267606797
23andMe allrs267606797
SNP Nexus

SNPshotrs267606797
SNPdbers267606797
MSV3drs267606797
GWAS Ctlgrs267606797
Max Magnitude0
ClinVar
Risk rs267606797(G;G)
Alt rs267606797(G;G)
Reference rs267606797(T;T)
Significance Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48729559A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000017892.23,