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

rs2097603

From SNPedia

Merged intors2075507
Orientationplus
Stabilizedplus
Make rs2097603(A;A)
Make rs2097603(A;G)
Make rs2097603(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position19940569
GeneCOMT, TXNRD2
is asnp
is mentioned by
dbSNPrs2097603
ebirs2097603
HLIrs2097603
Exacrs2097603
Varsomers2097603
Maprs2097603
PheGenIrs2097603
hapmaprs2097603
1000 genomesrs2097603
hgdprs2097603
ensemblrs2097603
gopubmedrs2097603
geneviewrs2097603
scholarrs2097603
googlers2097603
pharmgkbrs2097603
gwascentralrs2097603
openSNPrs2097603
23andMers2097603
23andMe allrs2097603
SNP Nexus

SNPshotrs2097603
SNPdbers2097603
MSV3drs2097603
GWAS Ctlgrs2097603
StatusMerged into rs2075507
Max Magnitude
[PMID 19071221OA-icon.png] gray matter volume and interacts with rs2097603 related to extracellular dopamine

[PMID 19605537OA-icon.png] Effects of Catechol-O-Methyltransferase on Normal Variation in the Cognitive Function of Children

[PMID 24862404] Exploring the indirect effects of catechol-O-methyltransferase (COMT) genotype on psychotic experiences through cognitive function and anxiety disorders in a large birth cohort of children