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rs267606796

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606796(A;A)
Make rs267606796(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48411338
GeneFBN1
is asnp
is mentioned by
dbSNPrs267606796
ebirs267606796
HLIrs267606796
Exacrs267606796
Varsomers267606796
Maprs267606796
PheGenIrs267606796
hapmaprs267606796
1000 genomesrs267606796
hgdprs267606796
ensemblrs267606796
gopubmedrs267606796
geneviewrs267606796
scholarrs267606796
googlers267606796
pharmgkbrs267606796
gwascentralrs267606796
openSNPrs267606796
23andMers267606796
23andMe allrs267606796
SNP Nexus

SNPshotrs267606796
SNPdbers267606796
MSV3drs267606796
GWAS Ctlgrs267606796
Max Magnitude0
ClinVar
Risk rs267606796(A;A)
Alt rs267606796(A;A)
Reference rs267606796(G;G)
Significance Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48703535C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017886.27,