rs34069356

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs34069356(A;A)

Make rs34069356(A;G)

Reference

GRCh38 38.1/142

Chromosome

20

Position

58995705

Gene

CTSZ

is a	snp
is	mentioned by
dbSNP	rs34069356
dbSNP (classic)	rs34069356
ClinGen	rs34069356
ebi	rs34069356
HLI	rs34069356
Exac	rs34069356
Gnomad	rs34069356
Varsome	rs34069356
LitVar	rs34069356
Map	rs34069356
PheGenI	rs34069356
Biobank	rs34069356
1000 genomes	rs34069356
hgdp	rs34069356
ensembl	rs34069356
geneview	rs34069356
scholar	rs34069356
google	rs34069356
pharmgkb	rs34069356
gwascentral	rs34069356
openSNP	rs34069356
23andMe	rs34069356
SNPshot	rs34069356
SNPdbe	rs34069356
MSV3d	rs34069356
GWAS Ctlg	rs34069356

GMAF

0.002755

Max Magnitude

0

OMIM	155540
Desc	MELANOCORTIN 3 RECEPTOR; MC3R
Variant
Related	also

OMIM	603169
Desc	CATHEPSIN Z; CTSZ
Variant
Related	also

OMIM	612929
Desc
Variant
Related	also

[PMID 21368909] Polymorphisms in MC3R promoter and CTSZ 3'UTR are associated with tuberculosis susceptibility.

[PMID 23827504] Association of CTSZ rs34069356 and MC3R rs6127698 gene polymorphisms with pulmonary tuberculosis