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rs193922234

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922234(G;G)
Make rs193922234(G;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position48421591
GeneFBN1
is asnp
is mentioned by
dbSNPrs193922234
ebirs193922234
HLIrs193922234
Exacrs193922234
Varsomers193922234
Maprs193922234
PheGenIrs193922234
hapmaprs193922234
1000 genomesrs193922234
hgdprs193922234
ensemblrs193922234
gopubmedrs193922234
geneviewrs193922234
scholarrs193922234
googlers193922234
pharmgkbrs193922234
gwascentralrs193922234
openSNPrs193922234
23andMers193922234
23andMe allrs193922234
SNP Nexus

SNPshotrs193922234
SNPdbers193922234
MSV3drs193922234
GWAS Ctlgrs193922234
Max Magnitude0
ClinVar
Risk rs193922234(G;G)
Alt rs193922234(G;G)
Reference rs193922234(T;T)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48713788A>C
CLNSRC ClinVar LabCorp
CLNACC RCV000029778.1,