rs137853123

Orientation

minus

Stabilized

minus

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

Make rs137853123(C;T)

Make rs137853123(T;T)

Reference

GRCh38 38.1/141

Chromosome

22

Position

37070557

Gene

TMPRSS6

is a	snp
is	mentioned by
dbSNP	rs137853123
dbSNP (classic)	rs137853123
ClinGen	rs137853123
ebi	rs137853123
HLI	rs137853123
Exac	rs137853123
Gnomad	rs137853123
Varsome	rs137853123
LitVar	rs137853123
Map	rs137853123
PheGenI	rs137853123
Biobank	rs137853123
1000 genomes	rs137853123
hgdp	rs137853123
ensembl	rs137853123
geneview	rs137853123
scholar	rs137853123
google	rs137853123
pharmgkb	rs137853123
gwascentral	rs137853123
openSNP	rs137853123
23andMe	rs137853123
SNPshot	rs137853123
SNPdbe	rs137853123
MSV3d	rs137853123
GWAS Ctlg	rs137853123

Max Magnitude

0

OMIM	609862
Desc
Variant	0010
Related	also

ClinVar
Risk	rs137853123(T;T)
Alt	rs137853123(T;T)
Reference	Rs137853123(C;C)
Significance	Pathogenic
Disease	Microcytic anemia
Variation	info
Gene	TMPRSS6
CLNDBN	Microcytic anemia
Reversed	1
HGVS	NC_000022.10:g.37466597G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000001473.3,