rs137853121

Orientation

minus

Stabilized

minus

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

Make rs137853121(A;A)

Make rs137853121(A;C)

Reference

GRCh38 38.1/141

Chromosome

22

Position

37084775

Gene

TMPRSS6

is a	snp
is	mentioned by
dbSNP	rs137853121
dbSNP (classic)	rs137853121
ClinGen	rs137853121
ebi	rs137853121
HLI	rs137853121
Exac	rs137853121
Gnomad	rs137853121
Varsome	rs137853121
LitVar	rs137853121
Map	rs137853121
PheGenI	rs137853121
Biobank	rs137853121
1000 genomes	rs137853121
hgdp	rs137853121
ensembl	rs137853121
geneview	rs137853121
scholar	rs137853121
google	rs137853121
pharmgkb	rs137853121
gwascentral	rs137853121
openSNP	rs137853121
23andMe	rs137853121
SNPshot	rs137853121
SNPdbe	rs137853121
MSV3d	rs137853121
GWAS Ctlg	rs137853121

GMAF

0.0009183

Max Magnitude

0

OMIM	609862
Desc
Variant	0007
Related	also

ClinVar
Risk	rs137853121(A;A)
Alt	rs137853121(A;A)
Reference	Rs137853121(C;C)
Significance	Pathogenic
Disease	Microcytic anemia
Variation	info
Gene	TMPRSS6
CLNDBN	Microcytic anemia
Reversed	1
HGVS	NC_000022.10:g.37480815G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000001470.3,