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rs727505006

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727505006(C;T)
Make rs727505006(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position48487402
GeneFBN1
is asnp
is mentioned by
dbSNPrs727505006
ebirs727505006
HLIrs727505006
Exacrs727505006
Varsomers727505006
Maprs727505006
PheGenIrs727505006
hapmaprs727505006
1000 genomesrs727505006
hgdprs727505006
ensemblrs727505006
gopubmedrs727505006
geneviewrs727505006
scholarrs727505006
googlers727505006
pharmgkbrs727505006
gwascentralrs727505006
openSNPrs727505006
23andMers727505006
23andMe allrs727505006
SNP Nexus

SNPshotrs727505006
SNPdbers727505006
MSV3drs727505006
GWAS Ctlgrs727505006
Max Magnitude0
ClinVar
Risk rs727505006(T;T)
Alt rs727505006(T;T)
Reference rs727505006(C;C)
Significance Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48779599G>A
CLNSRC
CLNACC RCV000156427.1,