Have questions? Visit https://www.reddit.com/r/SNPedia

rs193922207

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922207(A;A)
Make rs193922207(A;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position48468001
GeneFBN1
is asnp
is mentioned by
dbSNPrs193922207
ebirs193922207
HLIrs193922207
Exacrs193922207
Varsomers193922207
Maprs193922207
PheGenIrs193922207
hapmaprs193922207
1000 genomesrs193922207
hgdprs193922207
ensemblrs193922207
gopubmedrs193922207
geneviewrs193922207
scholarrs193922207
googlers193922207
pharmgkbrs193922207
gwascentralrs193922207
openSNPrs193922207
23andMers193922207
23andMe allrs193922207
SNP Nexus

SNPshotrs193922207
SNPdbers193922207
MSV3drs193922207
GWAS Ctlgrs193922207
Max Magnitude0
ClinVar
Risk rs193922207(A;A)
Alt rs193922207(A;A)
Reference rs193922207(T;T)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48760198A>T
CLNSRC ClinVar LabCorp
CLNACC RCV000029741.1,