rs786205057

Orientation

minus

Stabilized

minus

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

Make rs786205057(-;-)

Make rs786205057(-;G)

Reference

GRCh38.p2 38.2/146

Chromosome

22

Position

37070539

Gene

TMPRSS6

is a	snp
is	mentioned by
dbSNP	rs786205057
dbSNP (classic)	rs786205057
ClinGen	rs786205057
ebi	rs786205057
HLI	rs786205057
Exac	rs786205057
Gnomad	rs786205057
Varsome	rs786205057
LitVar	rs786205057
Map	rs786205057
PheGenI	rs786205057
Biobank	rs786205057
1000 genomes	rs786205057
hgdp	rs786205057
ensembl	rs786205057
geneview	rs786205057
scholar	rs786205057
google	rs786205057
pharmgkb	rs786205057
gwascentral	rs786205057
openSNP	rs786205057
23andMe	rs786205057
SNPshot	rs786205057
SNPdbe	rs786205057
MSV3d	rs786205057
GWAS Ctlg	rs786205057

Max Magnitude

0

ClinVar
Risk	rs786205057(-;-)
Alt	rs786205057(-;-)
Reference	Rs786205057(G;G)
Significance	Pathogenic
Disease	Microcytic anemia
Variation	info
Gene	TMPRSS6
CLNDBN	Microcytic anemia
Reversed	1
HGVS	NC_000022.10:g.37466579delC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000001465.4,