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rs17500488

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs17500488(C;C)
Make rs17500488(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position115669142
GeneVANGL1
is asnp
is mentioned by
dbSNPrs17500488
ebirs17500488
HLIrs17500488
Exacrs17500488
Varsomers17500488
Maprs17500488
PheGenIrs17500488
hapmaprs17500488
1000 genomesrs17500488
hgdprs17500488
ensemblrs17500488
gopubmedrs17500488
geneviewrs17500488
scholarrs17500488
googlers17500488
pharmgkbrs17500488
gwascentralrs17500488
openSNPrs17500488
23andMers17500488
23andMe allrs17500488
SNP Nexus

SNPshotrs17500488
SNPdbers17500488
MSV3drs17500488
GWAS Ctlgrs17500488
GMAF0.1047
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 21685173OA-icon.png] Common Variants in CASQ2, GPD1L and NOS1AP Are Significantly Associated with Risk of Sudden Death in Patients with Coronary Artery Disease