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rs17849308

From SNPedia

Merged intors4680
Orientationplus
Stabilizedplus
Make rs17849308(A;A)
Make rs17849308(A;G)
Make rs17849308(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position19963748
GeneCOMT, MIR4761
is asnp
is mentioned by
dbSNPrs17849308
ebirs17849308
HLIrs17849308
Exacrs17849308
Varsomers17849308
Maprs17849308
PheGenIrs17849308
hapmaprs17849308
1000 genomesrs17849308
hgdprs17849308
ensemblrs17849308
gopubmedrs17849308
geneviewrs17849308
scholarrs17849308
googlers17849308
pharmgkbrs17849308
gwascentralrs17849308
openSNPrs17849308
23andMers17849308
23andMe allrs17849308
SNP Nexus

SNPshotrs17849308
SNPdbers17849308
MSV3drs17849308
GWAS Ctlgrs17849308
StatusMerged into rs4680
Max Magnitude
? (A;A) (A;G) (G;G) 28
This is a mistaken rs#, apparently created by OMIM. It should refer to rs4680.
OMIM116790
DescCATECHOL-O-METHYLTRANSFERASE POLYMORPHISM
Variant0001
Relatedalso
Neighborrs4818
Distance63
Neighborrs4680
Distance1