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rs869025425

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869025425(-;-)
Make rs869025425(-;A)
Make rs869025425(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position48481725
GeneFBN1
is asnp
is mentioned by
dbSNPrs869025425
ebirs869025425
HLIrs869025425
Exacrs869025425
Varsomers869025425
Maprs869025425
PheGenIrs869025425
hapmaprs869025425
1000 genomesrs869025425
hgdprs869025425
ensemblrs869025425
gopubmedrs869025425
geneviewrs869025425
scholarrs869025425
googlers869025425
pharmgkbrs869025425
gwascentralrs869025425
openSNPrs869025425
23andMers869025425
23andMe allrs869025425
SNP Nexus

SNPshotrs869025425
SNPdbers869025425
MSV3drs869025425
GWAS Ctlgrs869025425
Max Magnitude0
ClinVar
Risk rs869025425(A;A)
Alt rs869025425(A;A)
Reference rs869025425(;)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48773923dupT
CLNSRC
CLNACC RCV000208271.1,