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rs9332377

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common/normal
Make rs9332377(C;T)
Make rs9332377(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position19968169
GeneARVCF, COMT
is asnp
is mentioned by
dbSNPrs9332377
dbSNP (classic)rs9332377
ClinGenrs9332377
ebirs9332377
HLIrs9332377
Exacrs9332377
Gnomadrs9332377
Varsomers9332377
LitVarrs9332377
Maprs9332377
PheGenIrs9332377
Biobankrs9332377
1000 genomesrs9332377
hgdprs9332377
ensemblrs9332377
geneviewrs9332377
scholarrs9332377
googlers9332377
pharmgkbrs9332377
gwascentralrs9332377
openSNPrs9332377
23andMers9332377
SNPshotrs9332377
SNPdbers9332377
MSV3drs9332377
GWAS Ctlgrs9332377
GMAF0.1584
Max Magnitude0
? (C;C) (C;T) (T;T) 28


OMIM613290
Desc
Variant
Relatedalso

[PMID 19015200OA-icon.png] Polymorphisms in estrogen- and androgen-metabolizing genes and the risk of gastric cancer. Found a statistically non-significant increased risk with rs9332377 (OR per variant allele of 1.24, 95% CI: 0.93–1.67).


[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

23andMe blog hearing loss linked to a chemotherapy drug named Cisplatin.


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