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rs193922198

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922198(-;-)
Make rs193922198(-;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48488383
GeneFBN1
is asnp
is mentioned by
dbSNPrs193922198
ebirs193922198
HLIrs193922198
Exacrs193922198
Varsomers193922198
Maprs193922198
PheGenIrs193922198
hapmaprs193922198
1000 genomesrs193922198
hgdprs193922198
ensemblrs193922198
gopubmedrs193922198
geneviewrs193922198
scholarrs193922198
googlers193922198
pharmgkbrs193922198
gwascentralrs193922198
openSNPrs193922198
23andMers193922198
23andMe allrs193922198
SNP Nexus

SNPshotrs193922198
SNPdbers193922198
MSV3drs193922198
GWAS Ctlgrs193922198
Max Magnitude0
ClinVar
Risk rs193922198(;)
Alt rs193922198(;)
Reference rs193922198(G;G)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48780580delC
CLNSRC ClinVar LabCorp
CLNACC RCV000029724.3,