rs9332377

plus

Geno	Mag	Summary
(C;C)	0	common/normal

Make rs9332377(C;T)

Make rs9332377(T;T)

Reference

GRCh38 38.1/141

Chromosome

22

Position

19968169

Gene	ARVCF, COMT

is a	snp
is	mentioned by
dbSNP	rs9332377
dbSNP (classic)	rs9332377
ClinGen	rs9332377
ebi	rs9332377
HLI	rs9332377
Exac	rs9332377
Gnomad	rs9332377
Varsome	rs9332377
LitVar	rs9332377
Map	rs9332377
PheGenI	rs9332377
Biobank	rs9332377
1000 genomes	rs9332377
hgdp	rs9332377
ensembl	rs9332377
geneview	rs9332377
scholar	rs9332377
google	rs9332377
pharmgkb	rs9332377
gwascentral	rs9332377
openSNP	rs9332377
23andMe	rs9332377
SNPshot	rs9332377
SNPdbe	rs9332377
MSV3d	rs9332377
GWAS Ctlg	rs9332377

GMAF

0.1584

Max Magnitude

0

?

(C;C) (C;T) (T;T)

28

OMIM	613290
Desc
Variant
Related	also

[PMID 19015200 ] 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 18436194 ] Catechol-O-methyltransferase contributes to genetic susceptibility shared among anxiety spectrum phenotypes.

[PMID 18937309 ] 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.