rs137853122

Orientation

minus

Stabilized

minus

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

Make rs137853122(G;G)

Make rs137853122(G;T)

Reference

GRCh38 38.1/141

Chromosome

22

Position

37084339

Gene

TMPRSS6

is a	snp
is	mentioned by
dbSNP	rs137853122
dbSNP (classic)	rs137853122
ClinGen	rs137853122
ebi	rs137853122
HLI	rs137853122
Exac	rs137853122
Gnomad	rs137853122
Varsome	rs137853122
LitVar	rs137853122
Map	rs137853122
PheGenI	rs137853122
Biobank	rs137853122
1000 genomes	rs137853122
hgdp	rs137853122
ensembl	rs137853122
geneview	rs137853122
scholar	rs137853122
google	rs137853122
pharmgkb	rs137853122
gwascentral	rs137853122
openSNP	rs137853122
23andMe	rs137853122
SNPshot	rs137853122
SNPdbe	rs137853122
MSV3d	rs137853122
GWAS Ctlg	rs137853122

Max Magnitude

0

OMIM	609862
Desc
Variant	0009
Related	also

ClinVar
Risk	rs137853122(G;G)
Alt	rs137853122(G;G)
Reference	Rs137853122(T;T)
Significance	Pathogenic
Disease	Microcytic anemia
Variation	info
Gene	TMPRSS6
CLNDBN	Microcytic anemia
Reversed	1
HGVS	NC_000022.10:g.37480379A>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000001472.4,