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rs193922233

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922233(C;G)
Make rs193922233(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48425410
GeneFBN1
is asnp
is mentioned by
dbSNPrs193922233
ebirs193922233
HLIrs193922233
Exacrs193922233
Varsomers193922233
Maprs193922233
PheGenIrs193922233
hapmaprs193922233
1000 genomesrs193922233
hgdprs193922233
ensemblrs193922233
gopubmedrs193922233
geneviewrs193922233
scholarrs193922233
googlers193922233
pharmgkbrs193922233
gwascentralrs193922233
openSNPrs193922233
23andMers193922233
23andMe allrs193922233
SNP Nexus

SNPshotrs193922233
SNPdbers193922233
MSV3drs193922233
GWAS Ctlgrs193922233
Max Magnitude0
ClinVar
Risk rs193922233(G;G)
Alt rs193922233(G;G)
Reference rs193922233(C;C)
Significance Probable-Pathogenic
Disease Marfan syndrome not specified
Variation info
Gene FBN1
CLNDBN Marfan syndrome not specified
Reversed 1
HGVS NC_000015.9:g.48717607G>C
CLNSRC ClinVar LabCorp
CLNACC RCV000029777.1, RCV000181602.2,