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rs2230267

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0.5 benign most likely
(C;T) 0.5 benign most likely
(T;T) 0 common in clinvar
ReferenceGRCh38 38.1/142
Chromosome19
Position48965830
GeneFTL
is asnp
is mentioned by
dbSNPrs2230267
ebirs2230267
HLIrs2230267
Exacrs2230267
Varsomers2230267
Maprs2230267
PheGenIrs2230267
hapmaprs2230267
1000 genomesrs2230267
hgdprs2230267
ensemblrs2230267
gopubmedrs2230267
geneviewrs2230267
scholarrs2230267
googlers2230267
pharmgkbrs2230267
gwascentralrs2230267
openSNPrs2230267
23andMers2230267
23andMe allrs2230267
SNP Nexus

SNPshotrs2230267
SNPdbers2230267
MSV3drs2230267
GWAS Ctlgrs2230267
Max Magnitude0.5
ClinVar
Risk rs2230267(C;C)
Alt rs2230267(C;C)
Reference rs2230267(T;T)
Significance Probable-Pathogenic
Disease sporadic abdominal aortic aneurysm not specified
Variation info
Gene FTL
CLNDBN sporadic abdominal aortic aneurysm not specified
Reversed 0
HGVS NC_000019.9:g.49469087T>C
CLNSRC ClinVar University of Chicago
CLNACC RCV000144503.1, RCV000146000.1,