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rs5993890

From SNPedia

Orientationplus
Stabilizedplus
Make rs5993890(A;A)
Make rs5993890(A;G)
Make rs5993890(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position19971306
GeneARVCF
is asnp
is mentioned by
dbSNPrs5993890
ebirs5993890
HLIrs5993890
Exacrs5993890
Varsomers5993890
Maprs5993890
PheGenIrs5993890
hapmaprs5993890
1000 genomesrs5993890
hgdprs5993890
ensemblrs5993890
gopubmedrs5993890
geneviewrs5993890
scholarrs5993890
googlers5993890
pharmgkbrs5993890
gwascentralrs5993890
openSNPrs5993890
23andMers5993890
23andMe allrs5993890
SNP Nexus

SNPshotrs5993890
SNPdbers5993890
MSV3drs5993890
GWAS Ctlgrs5993890
GMAF0.07117
Max Magnitude

[PMID 20333729OA-icon.png] A functional variant provided further evidence for the association of ARVCF with schizophrenia