rs536522394

Orientation

plus

Stabilized

plus

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

Make rs536522394(-;-)

Make rs536522394(-;TACCTTGGGTTGGG)

Make rs536522394(TACCTTGGGTTGGG;TACCTTGGGTTGGG)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

58273467

Gene

MPO

is a	snp
is	mentioned by
dbSNP	rs536522394
dbSNP (classic)	rs536522394
ClinGen	rs536522394
ebi	rs536522394
HLI	rs536522394
Exac	rs536522394
Gnomad	rs536522394
Varsome	rs536522394
LitVar	rs536522394
Map	rs536522394
PheGenI	rs536522394
Biobank	rs536522394
1000 genomes	rs536522394
hgdp	rs536522394
ensembl	rs536522394
geneview	rs536522394
scholar	rs536522394
google	rs536522394
pharmgkb	rs536522394
gwascentral	rs536522394
openSNP	rs536522394
23andMe	rs536522394
SNPshot	rs536522394
SNPdbe	rs536522394
MSV3d	rs536522394
GWAS Ctlg	rs536522394

Max Magnitude

0

ClinVar
Risk	rs536522394(-;-)
Alt	rs536522394(-;-)
Reference	Rs536522394(GGGTTGGGTTCCAT;GGGTTGGGTTCCAT)
Significance	Other
Disease	Myeloperoxidase deficiency not provided
Variation	info
Gene	MPO
CLNDBN	Myeloperoxidase deficiency not provided
Reversed	0
HGVS	NC_000017.10:g.56350828_56350841delGGGTTGGGTTCCAT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003813.4, RCV000274466.1,