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rs193922236

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922236(A;A)
Make rs193922236(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48420700
GeneFBN1
is asnp
is mentioned by
dbSNPrs193922236
ebirs193922236
HLIrs193922236
Exacrs193922236
Varsomers193922236
Maprs193922236
PheGenIrs193922236
hapmaprs193922236
1000 genomesrs193922236
hgdprs193922236
ensemblrs193922236
gopubmedrs193922236
geneviewrs193922236
scholarrs193922236
googlers193922236
pharmgkbrs193922236
gwascentralrs193922236
openSNPrs193922236
23andMers193922236
23andMe allrs193922236
SNP Nexus

SNPshotrs193922236
SNPdbers193922236
MSV3drs193922236
GWAS Ctlgrs193922236
Max Magnitude0
ClinVar
Risk rs193922236(A;A)
Alt rs193922236(A;A)
Reference rs193922236(G;G)
Significance Pathogenic
Disease Marfan syndrome not provided
Variation info
Gene FBN1
CLNDBN Marfan syndrome not provided
Reversed 1
HGVS NC_000015.9:g.48712897C>T
CLNSRC ClinVar
CLNACC RCV000029781.1, RCV000181599.2,