rs13306278

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs13306278(C;T)

Make rs13306278(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

22

Position

19941504

Gene	COMT, TXNRD2

is a	snp
is	mentioned by
dbSNP	rs13306278
dbSNP (classic)	rs13306278
ClinGen	rs13306278
ebi	rs13306278
HLI	rs13306278
Exac	rs13306278
Gnomad	rs13306278
Varsome	rs13306278
LitVar	rs13306278
Map	rs13306278
PheGenI	rs13306278
Biobank	rs13306278
1000 genomes	rs13306278
hgdp	rs13306278
ensembl	rs13306278
geneview	rs13306278
scholar	rs13306278
google	rs13306278
pharmgkb	rs13306278
gwascentral	rs13306278
openSNP	rs13306278
23andMe	rs13306278
SNPshot	rs13306278
SNPdbe	rs13306278
MSV3d	rs13306278
GWAS Ctlg	rs13306278

Max Magnitude

0

ClinVar
Risk	rs13306278(T;T)
Alt	rs13306278(T;T)
Reference	Rs13306278(C;C)
Significance	Drug-response
Disease	Selective serotonin reuptake inhibitors response - Efficacy
Variation	info
Gene	TXNRD2 COMT
CLNDBN	Selective serotonin reuptake inhibitors response - Efficacy
Reversed	0
HGVS	NC_000022.10:g.19929027C>T
CLNSRC	PharmGKB Clinical Annotation
CLNACC	RCV000211312.1,