rs786205059

Orientation

minus

Stabilized

minus

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

Make rs786205059(C;C)

Make rs786205059(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

22

Position

37069072

Gene

TMPRSS6

is a	snp
is	mentioned by
dbSNP	rs786205059
dbSNP (classic)	rs786205059
ClinGen	rs786205059
ebi	rs786205059
HLI	rs786205059
Exac	rs786205059
Gnomad	rs786205059
Varsome	rs786205059
LitVar	rs786205059
Map	rs786205059
PheGenI	rs786205059
Biobank	rs786205059
1000 genomes	rs786205059
hgdp	rs786205059
ensembl	rs786205059
geneview	rs786205059
scholar	rs786205059
google	rs786205059
pharmgkb	rs786205059
gwascentral	rs786205059
openSNP	rs786205059
23andMe	rs786205059
SNPshot	rs786205059
SNPdbe	rs786205059
MSV3d	rs786205059
GWAS Ctlg	rs786205059

Max Magnitude

0

ClinVar
Risk	rs786205059(C;C)
Alt	rs786205059(C;C)
Reference	Rs786205059(G;G)
Significance	Pathogenic
Disease	Microcytic anemia
Variation	info
Gene	TMPRSS6
CLNDBN	Microcytic anemia
Reversed	1
HGVS	NC_000022.10:g.37465112C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000001467.4,