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rs869025426

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869025426(-;-)
Make rs869025426(-;T)
Make rs869025426(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position48463947
GeneFBN1
is asnp
is mentioned by
dbSNPrs869025426
ebirs869025426
HLIrs869025426
Exacrs869025426
Varsomers869025426
Maprs869025426
PheGenIrs869025426
hapmaprs869025426
1000 genomesrs869025426
hgdprs869025426
ensemblrs869025426
gopubmedrs869025426
geneviewrs869025426
scholarrs869025426
googlers869025426
pharmgkbrs869025426
gwascentralrs869025426
openSNPrs869025426
23andMers869025426
23andMe allrs869025426
SNP Nexus

SNPshotrs869025426
SNPdbers869025426
MSV3drs869025426
GWAS Ctlgrs869025426
Max Magnitude0
ClinVar
Risk rs869025426(T;T)
Alt rs869025426(T;T)
Reference rs869025426(;)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48756145dupA
CLNSRC
CLNACC RCV000208525.1,