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rs992690

From SNPedia

Orientationplus
Stabilizedplus
Make rs992690(G;G)
Make rs992690(G;T)
Make rs992690(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position16497227
is asnp
is mentioned by
dbSNPrs992690
ebirs992690
HLIrs992690
Exacrs992690
Varsomers992690
Maprs992690
PheGenIrs992690
hapmaprs992690
1000 genomesrs992690
hgdprs992690
ensemblrs992690
gopubmedrs992690
geneviewrs992690
scholarrs992690
googlers992690
pharmgkbrs992690
gwascentralrs992690
openSNPrs992690
23andMers992690
23andMe allrs992690
SNP Nexus

SNPshotrs992690
SNPdbers992690
MSV3drs992690
GWAS Ctlgrs992690
GMAF0.242
Max Magnitude
? (G;G) (G;T) (T;T) 28

[PMID 23450469] [Genome-wide linkage scan for an ethnic Han Chinese pedigree affected with schizophrenia]