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rs193922187

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922187(-;-)
Make rs193922187(-;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position48497373
GeneFBN1
is asnp
is mentioned by
dbSNPrs193922187
ebirs193922187
HLIrs193922187
Exacrs193922187
Varsomers193922187
Maprs193922187
PheGenIrs193922187
hapmaprs193922187
1000 genomesrs193922187
hgdprs193922187
ensemblrs193922187
gopubmedrs193922187
geneviewrs193922187
scholarrs193922187
googlers193922187
pharmgkbrs193922187
gwascentralrs193922187
openSNPrs193922187
23andMers193922187
23andMe allrs193922187
SNP Nexus

SNPshotrs193922187
SNPdbers193922187
MSV3drs193922187
GWAS Ctlgrs193922187
Max Magnitude0
ClinVar
Risk rs193922187(;)
Alt rs193922187(;)
Reference rs193922187(T;T)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48789570delA
CLNSRC ClinVar LabCorp
CLNACC RCV000029706.1,