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rs869025408

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869025408(A;G)
Make rs869025408(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position48465791
GeneFBN1
is asnp
is mentioned by
dbSNPrs869025408
ebirs869025408
HLIrs869025408
Exacrs869025408
Varsomers869025408
Maprs869025408
PheGenIrs869025408
hapmaprs869025408
1000 genomesrs869025408
hgdprs869025408
ensemblrs869025408
gopubmedrs869025408
geneviewrs869025408
scholarrs869025408
googlers869025408
pharmgkbrs869025408
gwascentralrs869025408
openSNPrs869025408
23andMers869025408
23andMe allrs869025408
SNP Nexus

SNPshotrs869025408
SNPdbers869025408
MSV3drs869025408
GWAS Ctlgrs869025408
Max Magnitude0
ClinVar
Risk rs869025408(G;G)
Alt rs869025408(G;G)
Reference rs869025408(A;A)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48757988T>C
CLNSRC
CLNACC RCV000208162.1,