rs17849308

Merged into

rs4680

Orientation

plus

Stabilized

plus

Make rs17849308(A;A)

Make rs17849308(A;G)

Make rs17849308(G;G)

Reference

GRCh38 38.1/141

Chromosome

22

Position

19963748

Gene	COMT, MIR4761

is a	snp
is	mentioned by
dbSNP	rs17849308
dbSNP (classic)	rs17849308
ClinGen	rs17849308
ebi	rs17849308
HLI	rs17849308
Exac	rs17849308
Gnomad	rs17849308
Varsome	rs17849308
LitVar	rs17849308
Map	rs17849308
PheGenI	rs17849308
Biobank	rs17849308
1000 genomes	rs17849308
hgdp	rs17849308
ensembl	rs17849308
geneview	rs17849308
scholar	rs17849308
google	rs17849308
pharmgkb	rs17849308
gwascentral	rs17849308
openSNP	rs17849308
23andMe	rs17849308
SNPshot	rs17849308
SNPdbe	rs17849308
MSV3d	rs17849308
GWAS Ctlg	rs17849308

Status

Merged into rs4680

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

This is a mistaken rs#, apparently created by OMIM. It should refer to rs4680.

OMIM	116790
Desc	CATECHOL-O-METHYLTRANSFERASE POLYMORPHISM
Variant	0001
Related	also