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rs13306278

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs13306278(C;T)
Make rs13306278(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position19941504
GeneCOMT, TXNRD2
is asnp
is mentioned by
dbSNPrs13306278
ebirs13306278
HLIrs13306278
Exacrs13306278
Varsomers13306278
Maprs13306278
PheGenIrs13306278
hapmaprs13306278
1000 genomesrs13306278
hgdprs13306278
ensemblrs13306278
gopubmedrs13306278
geneviewrs13306278
scholarrs13306278
googlers13306278
pharmgkbrs13306278
gwascentralrs13306278
openSNPrs13306278
23andMers13306278
23andMe allrs13306278
SNP Nexus

SNPshotrs13306278
SNPdbers13306278
MSV3drs13306278
GWAS Ctlgrs13306278
Max Magnitude0
ClinVar
Risk rs13306278(T;T)
Alt rs13306278(T;T)
Reference rs13306278(C;C)
Significance Drug-response
Disease Selective serotonin reuptake inhibitors response - Efficacy
Variation info
Gene TXNRD2 COMT
CLNDBN Selective serotonin reuptake inhibitors response - Efficacy
Reversed 0
HGVS NC_000022.10:g.19929027C>T
CLNSRC PharmGKB Clinical Annotation PharmGKB
CLNACC RCV000211312.1,