Have questions? Visit https://www.reddit.com/r/SNPedia

rs193922179

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922179(A;A)
Make rs193922179(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48510124
GeneFBN1
is asnp
is mentioned by
dbSNPrs193922179
ebirs193922179
HLIrs193922179
Exacrs193922179
Varsomers193922179
Maprs193922179
PheGenIrs193922179
hapmaprs193922179
1000 genomesrs193922179
hgdprs193922179
ensemblrs193922179
gopubmedrs193922179
geneviewrs193922179
scholarrs193922179
googlers193922179
pharmgkbrs193922179
gwascentralrs193922179
openSNPrs193922179
23andMers193922179
23andMe allrs193922179
SNP Nexus

SNPshotrs193922179
SNPdbers193922179
MSV3drs193922179
GWAS Ctlgrs193922179
Max Magnitude0
ClinVar
Risk rs193922179(A;A)
Alt rs193922179(A;A)
Reference rs193922179(G;G)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48802321C>T
CLNSRC ClinVar LabCorp
CLNACC RCV000029694.1,