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rs193922206

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922206(A;T)
Make rs193922206(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position48596367
GeneFBN1
is asnp
is mentioned by
dbSNPrs193922206
ebirs193922206
HLIrs193922206
Exacrs193922206
Varsomers193922206
Maprs193922206
PheGenIrs193922206
hapmaprs193922206
1000 genomesrs193922206
hgdprs193922206
ensemblrs193922206
gopubmedrs193922206
geneviewrs193922206
scholarrs193922206
googlers193922206
pharmgkbrs193922206
gwascentralrs193922206
openSNPrs193922206
23andMers193922206
23andMe allrs193922206
SNP Nexus

SNPshotrs193922206
SNPdbers193922206
MSV3drs193922206
GWAS Ctlgrs193922206
Max Magnitude0
ClinVar
Risk rs193922206(T;T)
Alt rs193922206(T;T)
Reference rs193922206(A;A)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48888564T>A
CLNSRC ClinVar LabCorp
CLNACC RCV000029739.1,