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rs165656

From SNPedia

Orientationplus
Stabilizedplus
Make rs165656(C;C)
Make rs165656(C;G)
Make rs165656(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position19961340
GeneCOMT
is asnp
is mentioned by
dbSNPrs165656
dbSNP (old)rs165656
ClinGenrs165656
ebirs165656
HLIrs165656
Exacrs165656
Gnomadrs165656
Varsomers165656
Maprs165656
PheGenIrs165656
Biobankrs165656
1000 genomesrs165656
hgdprs165656
ensemblrs165656
gopubmedrs165656
geneviewrs165656
scholarrs165656
googlers165656
pharmgkbrs165656
gwascentralrs165656
openSNPrs165656
23andMers165656
23andMe allrs165656
SNP Nexus

SNPshotrs165656
SNPdbers165656
MSV3drs165656
GWAS Ctlgrs165656
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 23446089] Catechol-O-methyltransferase (COMT) gene polymorphisms as risk factor in temporomandibular disorders patients from Southern Italy