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rs9332377

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0
Make rs9332377(C;T)
Make rs9332377(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position19968169
GeneARVCF, COMT
is asnp
is mentioned by
dbSNPrs9332377
ebirs9332377
HLIrs9332377
Exacrs9332377
Varsomers9332377
Maprs9332377
PheGenIrs9332377
hapmaprs9332377
1000 genomesrs9332377
hgdprs9332377
ensemblrs9332377
gopubmedrs9332377
geneviewrs9332377
scholarrs9332377
googlers9332377
pharmgkbrs9332377
gwascentralrs9332377
openSNPrs9332377
23andMers9332377
23andMe allrs9332377
SNP Nexus

SNPshotrs9332377
SNPdbers9332377
MSV3drs9332377
GWAS Ctlgrs9332377
GMAF0.1584
Max Magnitude0
? (C;C) (C;T) (T;T) 28
23andMe blog hearing loss linked to a chemotherapy drug named Cisplatin.


[PMID 20979063] Why do young women smoke? VII COMT as a risk modifying gene for Nicotine dependence - role of gene-gene interaction, personality, and environmental factors


OMIM613290
Desc
Variant
Relatedalso
[PMID 18436194OA-icon.png] Catechol-O-methyltransferase contributes to genetic susceptibility shared among anxiety spectrum phenotypes.


[PMID 18937309OA-icon.png] Sexually dimorphic effects of four genes (COMT, SLC6A2, MAOA, SLC6A4) in genetic associations of ADHD: a preliminary study.


[PMID 19015200OA-icon.png] Polymorphisms in estrogen- and androgen-metabolizing genes and the risk of gastric cancer.


[PMID 20667552] Catechol-o-methyltransferase gene modulation on suicidal behavior and personality traits: review, meta-analysis and association study.


GET Evidence
rs9332377
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.179688
summary